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NM_007294.4(BRCA1):c.4358C>G (p.Ala1453Gly) AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Feb 28, 2022
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV002332310.2

Allele description [Variation Report for NM_007294.4(BRCA1):c.4358C>G (p.Ala1453Gly)]

NM_007294.4(BRCA1):c.4358C>G (p.Ala1453Gly)

Gene:
BRCA1:BRCA1 DNA repair associated [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17q21.31
Genomic location:
Preferred name:
NM_007294.4(BRCA1):c.4358C>G (p.Ala1453Gly)
HGVS:
  • NC_000017.11:g.43076614G>C
  • NG_005905.2:g.141370C>G
  • NM_001407571.1:c.4145C>G
  • NM_001407581.1:c.4424C>G
  • NM_001407582.1:c.4424C>G
  • NM_001407583.1:c.4424-3C>G
  • NM_001407585.1:c.4424-3C>G
  • NM_001407587.1:c.4421C>G
  • NM_001407590.1:c.4421-3C>G
  • NM_001407591.1:c.4421-3C>G
  • NM_001407593.1:c.4358C>G
  • NM_001407594.1:c.4358C>G
  • NM_001407596.1:c.4358C>G
  • NM_001407597.1:c.4358C>G
  • NM_001407598.1:c.4358C>G
  • NM_001407602.1:c.4358C>G
  • NM_001407603.1:c.4358C>G
  • NM_001407605.1:c.4358C>G
  • NM_001407610.1:c.4355C>G
  • NM_001407611.1:c.4355C>G
  • NM_001407612.1:c.4355C>G
  • NM_001407613.1:c.4355C>G
  • NM_001407614.1:c.4355C>G
  • NM_001407615.1:c.4355C>G
  • NM_001407616.1:c.4358-3C>G
  • NM_001407617.1:c.4358-3C>G
  • NM_001407618.1:c.4358-3C>G
  • NM_001407619.1:c.4358-3C>G
  • NM_001407620.1:c.4358-3C>G
  • NM_001407621.1:c.4358-3C>G
  • NM_001407622.1:c.4358-3C>G
  • NM_001407623.1:c.4358-3C>G
  • NM_001407624.1:c.4355C>G
  • NM_001407625.1:c.4355C>G
  • NM_001407626.1:c.4355C>G
  • NM_001407627.1:c.4352C>G
  • NM_001407628.1:c.4352C>G
  • NM_001407629.1:c.4352C>G
  • NM_001407630.1:c.4352C>G
  • NM_001407631.1:c.4352C>G
  • NM_001407632.1:c.4352C>G
  • NM_001407633.1:c.4355-3C>G
  • NM_001407634.1:c.4355-3C>G
  • NM_001407635.1:c.4355-3C>G
  • NM_001407636.1:c.4355-3C>G
  • NM_001407637.1:c.4355-3C>G
  • NM_001407638.1:c.4355-3C>G
  • NM_001407639.1:c.4355-3C>G
  • NM_001407640.1:c.4355-3C>G
  • NM_001407641.1:c.4355-3C>G
  • NM_001407642.1:c.4355-3C>G
  • NM_001407644.1:c.4352-3C>G
  • NM_001407645.1:c.4352-3C>G
  • NM_001407646.1:c.4346C>G
  • NM_001407647.1:c.4346-3C>G
  • NM_001407648.1:c.4301C>G
  • NM_001407649.1:c.4298C>G
  • NM_001407652.1:c.4358C>G
  • NM_001407653.1:c.4280C>G
  • NM_001407654.1:c.4280C>G
  • NM_001407655.1:c.4280C>G
  • NM_001407656.1:c.4277C>G
  • NM_001407657.1:c.4280-3C>G
  • NM_001407658.1:c.4280-3C>G
  • NM_001407659.1:c.4274C>G
  • NM_001407660.1:c.4274C>G
  • NM_001407661.1:c.4277-3C>G
  • NM_001407662.1:c.4277-3C>G
  • NM_001407663.1:c.4277-3C>G
  • NM_001407664.1:c.4235C>G
  • NM_001407665.1:c.4235C>G
  • NM_001407666.1:c.4235C>G
  • NM_001407667.1:c.4235C>G
  • NM_001407668.1:c.4235C>G
  • NM_001407669.1:c.4235C>G
  • NM_001407670.1:c.4232C>G
  • NM_001407671.1:c.4232C>G
  • NM_001407672.1:c.4232C>G
  • NM_001407673.1:c.4232C>G
  • NM_001407674.1:c.4232C>G
  • NM_001407675.1:c.4232C>G
  • NM_001407676.1:c.4232C>G
  • NM_001407677.1:c.4235-3C>G
  • NM_001407678.1:c.4235-3C>G
  • NM_001407679.1:c.4235-3C>G
  • NM_001407680.1:c.4235-3C>G
  • NM_001407681.1:c.4232-3C>G
  • NM_001407682.1:c.4232-3C>G
  • NM_001407683.1:c.4232-3C>G
  • NM_001407684.1:c.4358C>G
  • NM_001407685.1:c.4229C>G
  • NM_001407686.1:c.4229C>G
  • NM_001407687.1:c.4229C>G
  • NM_001407688.1:c.4232-3C>G
  • NM_001407689.1:c.4232-3C>G
  • NM_001407690.1:c.4229-3C>G
  • NM_001407691.1:c.4229-3C>G
  • NM_001407692.1:c.4217C>G
  • NM_001407694.1:c.4217C>G
  • NM_001407695.1:c.4217C>G
  • NM_001407696.1:c.4217C>G
  • NM_001407697.1:c.4217C>G
  • NM_001407698.1:c.4217C>G
  • NM_001407724.1:c.4217C>G
  • NM_001407725.1:c.4217C>G
  • NM_001407726.1:c.4217C>G
  • NM_001407727.1:c.4217C>G
  • NM_001407728.1:c.4217C>G
  • NM_001407729.1:c.4217C>G
  • NM_001407730.1:c.4217C>G
  • NM_001407731.1:c.4217C>G
  • NM_001407732.1:c.4217-3C>G
  • NM_001407733.1:c.4217-3C>G
  • NM_001407734.1:c.4217-3C>G
  • NM_001407735.1:c.4217-3C>G
  • NM_001407736.1:c.4217-3C>G
  • NM_001407737.1:c.4217-3C>G
  • NM_001407738.1:c.4217-3C>G
  • NM_001407739.1:c.4217-3C>G
  • NM_001407740.1:c.4214C>G
  • NM_001407741.1:c.4214C>G
  • NM_001407742.1:c.4214C>G
  • NM_001407743.1:c.4214C>G
  • NM_001407744.1:c.4214C>G
  • NM_001407745.1:c.4214C>G
  • NM_001407746.1:c.4214C>G
  • NM_001407747.1:c.4214C>G
  • NM_001407748.1:c.4214C>G
  • NM_001407749.1:c.4214C>G
  • NM_001407750.1:c.4214C>G
  • NM_001407751.1:c.4214C>G
  • NM_001407752.1:c.4214C>G
  • NM_001407838.1:c.4214-3C>G
  • NM_001407839.1:c.4214-3C>G
  • NM_001407841.1:c.4214-3C>G
  • NM_001407842.1:c.4214-3C>G
  • NM_001407843.1:c.4214-3C>G
  • NM_001407844.1:c.4214-3C>G
  • NM_001407845.1:c.4214-3C>G
  • NM_001407846.1:c.4214-3C>G
  • NM_001407847.1:c.4211C>G
  • NM_001407848.1:c.4211C>G
  • NM_001407849.1:c.4211C>G
  • NM_001407850.1:c.4214-3C>G
  • NM_001407851.1:c.4214-3C>G
  • NM_001407852.1:c.4214-3C>G
  • NM_001407853.1:c.4211C>G
  • NM_001407854.1:c.4358C>G
  • NM_001407858.1:c.4358-3C>G
  • NM_001407859.1:c.4358-3C>G
  • NM_001407860.1:c.4355C>G
  • NM_001407861.1:c.4355-3C>G
  • NM_001407862.1:c.4157C>G
  • NM_001407863.1:c.4235-3C>G
  • NM_001407874.1:c.4154-3C>G
  • NM_001407875.1:c.4154-3C>G
  • NM_001407879.1:c.4148C>G
  • NM_001407881.1:c.4148C>G
  • NM_001407882.1:c.4148C>G
  • NM_001407884.1:c.4148C>G
  • NM_001407885.1:c.4148C>G
  • NM_001407886.1:c.4148C>G
  • NM_001407887.1:c.4148C>G
  • NM_001407889.1:c.4148C>G
  • NM_001407894.1:c.4145C>G
  • NM_001407895.1:c.4145C>G
  • NM_001407896.1:c.4145C>G
  • NM_001407897.1:c.4145C>G
  • NM_001407898.1:c.4145C>G
  • NM_001407899.1:c.4145C>G
  • NM_001407900.1:c.4148-3C>G
  • NM_001407902.1:c.4148-3C>G
  • NM_001407904.1:c.4148-3C>G
  • NM_001407906.1:c.4148-3C>G
  • NM_001407907.1:c.4145C>G
  • NM_001407908.1:c.4145C>G
  • NM_001407909.1:c.4145C>G
  • NM_001407910.1:c.4145C>G
  • NM_001407915.1:c.4142C>G
  • NM_001407916.1:c.4145-3C>G
  • NM_001407917.1:c.4145-3C>G
  • NM_001407918.1:c.4145-3C>G
  • NM_001407919.1:c.4235C>G
  • NM_001407920.1:c.4094C>G
  • NM_001407921.1:c.4094C>G
  • NM_001407922.1:c.4094C>G
  • NM_001407923.1:c.4094C>G
  • NM_001407924.1:c.4094C>G
  • NM_001407925.1:c.4094C>G
  • NM_001407926.1:c.4094C>G
  • NM_001407927.1:c.4094-3C>G
  • NM_001407928.1:c.4094-3C>G
  • NM_001407929.1:c.4094-3C>G
  • NM_001407930.1:c.4091C>G
  • NM_001407931.1:c.4091C>G
  • NM_001407932.1:c.4091C>G
  • NM_001407933.1:c.4091C>G
  • NM_001407934.1:c.4088C>G
  • NM_001407935.1:c.4091-3C>G
  • NM_001407936.1:c.4091-3C>G
  • NM_001407937.1:c.4235C>G
  • NM_001407938.1:c.4235C>G
  • NM_001407939.1:c.4235-3C>G
  • NM_001407940.1:c.4232C>G
  • NM_001407941.1:c.4232-3C>G
  • NM_001407942.1:c.4217C>G
  • NM_001407943.1:c.4214C>G
  • NM_001407944.1:c.4217-3C>G
  • NM_001407945.1:c.4217-3C>G
  • NM_001407946.1:c.4025C>G
  • NM_001407947.1:c.4025C>G
  • NM_001407948.1:c.4025C>G
  • NM_001407949.1:c.4025C>G
  • NM_001407950.1:c.4025-3C>G
  • NM_001407951.1:c.4025-3C>G
  • NM_001407952.1:c.4022C>G
  • NM_001407953.1:c.4022C>G
  • NM_001407954.1:c.4022C>G
  • NM_001407955.1:c.4022C>G
  • NM_001407956.1:c.4019C>G
  • NM_001407957.1:c.4022-3C>G
  • NM_001407958.1:c.4022-3C>G
  • NM_001407959.1:c.3977C>G
  • NM_001407960.1:c.3977-3C>G
  • NM_001407962.1:c.3974C>G
  • NM_001407963.1:c.3974-3C>G
  • NM_001407964.1:c.4214-5376C>G
  • NM_001407965.1:c.3851C>G
  • NM_001407966.1:c.3470C>G
  • NM_001407967.1:c.3470-3C>G
  • NM_001407968.1:c.1754C>G
  • NM_001407969.1:c.1751C>G
  • NM_001407970.1:c.1115C>G
  • NM_001407971.1:c.1115C>G
  • NM_001407972.1:c.1112C>G
  • NM_001407973.1:c.1049C>G
  • NM_001407974.1:c.1049C>G
  • NM_001407975.1:c.1049C>G
  • NM_001407976.1:c.1049C>G
  • NM_001407977.1:c.1049C>G
  • NM_001407978.1:c.1049C>G
  • NM_001407979.1:c.1046C>G
  • NM_001407980.1:c.1046C>G
  • NM_001407981.1:c.1046C>G
  • NM_001407982.1:c.1046C>G
  • NM_001407983.1:c.1046C>G
  • NM_001407984.1:c.1046C>G
  • NM_001407985.1:c.1046C>G
  • NM_001407986.1:c.1046C>G
  • NM_001407990.1:c.1046C>G
  • NM_001407991.1:c.1046C>G
  • NM_001407992.1:c.1046C>G
  • NM_001407993.1:c.1049-3C>G
  • NM_001408392.1:c.1046-3C>G
  • NM_001408396.1:c.1046-3C>G
  • NM_001408397.1:c.1046-3C>G
  • NM_001408398.1:c.1046-3C>G
  • NM_001408399.1:c.1046-3C>G
  • NM_001408400.1:c.1043C>G
  • NM_001408401.1:c.1043C>G
  • NM_001408402.1:c.1043C>G
  • NM_001408403.1:c.1046-3C>G
  • NM_001408404.1:c.1046-3C>G
  • NM_001408406.1:c.1040C>G
  • NM_001408407.1:c.1043-3C>G
  • NM_001408408.1:c.1040C>G
  • NM_001408409.1:c.1037C>G
  • NM_001408410.1:c.974C>G
  • NM_001408411.1:c.971C>G
  • NM_001408412.1:c.971-3C>G
  • NM_001408413.1:c.968C>G
  • NM_001408414.1:c.971-3C>G
  • NM_001408415.1:c.971-3C>G
  • NM_001408416.1:c.968C>G
  • NM_001408418.1:c.932C>G
  • NM_001408419.1:c.932C>G
  • NM_001408420.1:c.932C>G
  • NM_001408421.1:c.929C>G
  • NM_001408422.1:c.932-3C>G
  • NM_001408423.1:c.932-3C>G
  • NM_001408424.1:c.929C>G
  • NM_001408425.1:c.926C>G
  • NM_001408426.1:c.926C>G
  • NM_001408427.1:c.926C>G
  • NM_001408428.1:c.926C>G
  • NM_001408429.1:c.926C>G
  • NM_001408430.1:c.926C>G
  • NM_001408431.1:c.929-3C>G
  • NM_001408432.1:c.923C>G
  • NM_001408433.1:c.923C>G
  • NM_001408434.1:c.923C>G
  • NM_001408435.1:c.923C>G
  • NM_001408436.1:c.926-3C>G
  • NM_001408437.1:c.926-3C>G
  • NM_001408438.1:c.926-3C>G
  • NM_001408439.1:c.926-3C>G
  • NM_001408440.1:c.926-3C>G
  • NM_001408441.1:c.923C>G
  • NM_001408442.1:c.923C>G
  • NM_001408443.1:c.923C>G
  • NM_001408444.1:c.923C>G
  • NM_001408445.1:c.923-3C>G
  • NM_001408446.1:c.923-3C>G
  • NM_001408447.1:c.923-3C>G
  • NM_001408448.1:c.923-3C>G
  • NM_001408450.1:c.923-3C>G
  • NM_001408451.1:c.914C>G
  • NM_001408452.1:c.908C>G
  • NM_001408453.1:c.908C>G
  • NM_001408454.1:c.908C>G
  • NM_001408455.1:c.908C>G
  • NM_001408456.1:c.908C>G
  • NM_001408457.1:c.908C>G
  • NM_001408458.1:c.908-3C>G
  • NM_001408459.1:c.908-3C>G
  • NM_001408460.1:c.908-3C>G
  • NM_001408461.1:c.908-3C>G
  • NM_001408462.1:c.905C>G
  • NM_001408463.1:c.905C>G
  • NM_001408464.1:c.905C>G
  • NM_001408465.1:c.905C>G
  • NM_001408466.1:c.905C>G
  • NM_001408467.1:c.905C>G
  • NM_001408468.1:c.905-3C>G
  • NM_001408469.1:c.905-3C>G
  • NM_001408470.1:c.902C>G
  • NM_001408472.1:c.1046C>G
  • NM_001408473.1:c.1046-3C>G
  • NM_001408474.1:c.848C>G
  • NM_001408475.1:c.845C>G
  • NM_001408476.1:c.848-3C>G
  • NM_001408478.1:c.839C>G
  • NM_001408479.1:c.839C>G
  • NM_001408480.1:c.839C>G
  • NM_001408481.1:c.839-3C>G
  • NM_001408482.1:c.839-3C>G
  • NM_001408483.1:c.839-3C>G
  • NM_001408484.1:c.839-3C>G
  • NM_001408485.1:c.839-3C>G
  • NM_001408489.1:c.836C>G
  • NM_001408490.1:c.836C>G
  • NM_001408491.1:c.836C>G
  • NM_001408492.1:c.836-3C>G
  • NM_001408493.1:c.836-3C>G
  • NM_001408494.1:c.809C>G
  • NM_001408495.1:c.806-3C>G
  • NM_001408496.1:c.785C>G
  • NM_001408497.1:c.785C>G
  • NM_001408498.1:c.785C>G
  • NM_001408499.1:c.785C>G
  • NM_001408500.1:c.785C>G
  • NM_001408501.1:c.785C>G
  • NM_001408502.1:c.782C>G
  • NM_001408503.1:c.782C>G
  • NM_001408504.1:c.782C>G
  • NM_001408505.1:c.782-3C>G
  • NM_001408506.1:c.722C>G
  • NM_001408507.1:c.719C>G
  • NM_001408508.1:c.710C>G
  • NM_001408509.1:c.710-3C>G
  • NM_001408510.1:c.668C>G
  • NM_001408511.1:c.665C>G
  • NM_001408512.1:c.545C>G
  • NM_001408513.1:c.836-5376C>G
  • NM_001408514.1:c.838+5790C>G
  • NM_007294.4:c.4358C>GMANE SELECT
  • NM_007297.4:c.4217C>G
  • NM_007298.4:c.1049-3C>G
  • NM_007299.4:c.1049-3C>G
  • NM_007300.4:c.4424-3C>G
  • NP_001394500.1:p.Ala1382Gly
  • NP_001394510.1:p.Ala1475Gly
  • NP_001394511.1:p.Ala1475Gly
  • NP_001394516.1:p.Ala1474Gly
  • NP_001394522.1:p.Ala1453Gly
  • NP_001394523.1:p.Ala1453Gly
  • NP_001394525.1:p.Ala1453Gly
  • NP_001394526.1:p.Ala1453Gly
  • NP_001394527.1:p.Ala1453Gly
  • NP_001394531.1:p.Ala1453Gly
  • NP_001394532.1:p.Ala1453Gly
  • NP_001394534.1:p.Ala1453Gly
  • NP_001394539.1:p.Ala1452Gly
  • NP_001394540.1:p.Ala1452Gly
  • NP_001394541.1:p.Ala1452Gly
  • NP_001394542.1:p.Ala1452Gly
  • NP_001394543.1:p.Ala1452Gly
  • NP_001394544.1:p.Ala1452Gly
  • NP_001394553.1:p.Ala1452Gly
  • NP_001394554.1:p.Ala1452Gly
  • NP_001394555.1:p.Ala1452Gly
  • NP_001394556.1:p.Ala1451Gly
  • NP_001394557.1:p.Ala1451Gly
  • NP_001394558.1:p.Ala1451Gly
  • NP_001394559.1:p.Ala1451Gly
  • NP_001394560.1:p.Ala1451Gly
  • NP_001394561.1:p.Ala1451Gly
  • NP_001394575.1:p.Ala1449Gly
  • NP_001394577.1:p.Ala1434Gly
  • NP_001394578.1:p.Ala1433Gly
  • NP_001394581.1:p.Ala1453Gly
  • NP_001394582.1:p.Ala1427Gly
  • NP_001394583.1:p.Ala1427Gly
  • NP_001394584.1:p.Ala1427Gly
  • NP_001394585.1:p.Ala1426Gly
  • NP_001394588.1:p.Ala1425Gly
  • NP_001394589.1:p.Ala1425Gly
  • NP_001394593.1:p.Ala1412Gly
  • NP_001394594.1:p.Ala1412Gly
  • NP_001394595.1:p.Ala1412Gly
  • NP_001394596.1:p.Ala1412Gly
  • NP_001394597.1:p.Ala1412Gly
  • NP_001394598.1:p.Ala1412Gly
  • NP_001394599.1:p.Ala1411Gly
  • NP_001394600.1:p.Ala1411Gly
  • NP_001394601.1:p.Ala1411Gly
  • NP_001394602.1:p.Ala1411Gly
  • NP_001394603.1:p.Ala1411Gly
  • NP_001394604.1:p.Ala1411Gly
  • NP_001394605.1:p.Ala1411Gly
  • NP_001394613.1:p.Ala1453Gly
  • NP_001394614.1:p.Ala1410Gly
  • NP_001394615.1:p.Ala1410Gly
  • NP_001394616.1:p.Ala1410Gly
  • NP_001394621.1:p.Ala1406Gly
  • NP_001394623.1:p.Ala1406Gly
  • NP_001394624.1:p.Ala1406Gly
  • NP_001394625.1:p.Ala1406Gly
  • NP_001394626.1:p.Ala1406Gly
  • NP_001394627.1:p.Ala1406Gly
  • NP_001394653.1:p.Ala1406Gly
  • NP_001394654.1:p.Ala1406Gly
  • NP_001394655.1:p.Ala1406Gly
  • NP_001394656.1:p.Ala1406Gly
  • NP_001394657.1:p.Ala1406Gly
  • NP_001394658.1:p.Ala1406Gly
  • NP_001394659.1:p.Ala1406Gly
  • NP_001394660.1:p.Ala1406Gly
  • NP_001394669.1:p.Ala1405Gly
  • NP_001394670.1:p.Ala1405Gly
  • NP_001394671.1:p.Ala1405Gly
  • NP_001394672.1:p.Ala1405Gly
  • NP_001394673.1:p.Ala1405Gly
  • NP_001394674.1:p.Ala1405Gly
  • NP_001394675.1:p.Ala1405Gly
  • NP_001394676.1:p.Ala1405Gly
  • NP_001394677.1:p.Ala1405Gly
  • NP_001394678.1:p.Ala1405Gly
  • NP_001394679.1:p.Ala1405Gly
  • NP_001394680.1:p.Ala1405Gly
  • NP_001394681.1:p.Ala1405Gly
  • NP_001394776.1:p.Ala1404Gly
  • NP_001394777.1:p.Ala1404Gly
  • NP_001394778.1:p.Ala1404Gly
  • NP_001394782.1:p.Ala1404Gly
  • NP_001394783.1:p.Ala1453Gly
  • NP_001394789.1:p.Ala1452Gly
  • NP_001394791.1:p.Ala1386Gly
  • NP_001394808.1:p.Ala1383Gly
  • NP_001394810.1:p.Ala1383Gly
  • NP_001394811.1:p.Ala1383Gly
  • NP_001394813.1:p.Ala1383Gly
  • NP_001394814.1:p.Ala1383Gly
  • NP_001394815.1:p.Ala1383Gly
  • NP_001394816.1:p.Ala1383Gly
  • NP_001394818.1:p.Ala1383Gly
  • NP_001394823.1:p.Ala1382Gly
  • NP_001394824.1:p.Ala1382Gly
  • NP_001394825.1:p.Ala1382Gly
  • NP_001394826.1:p.Ala1382Gly
  • NP_001394827.1:p.Ala1382Gly
  • NP_001394828.1:p.Ala1382Gly
  • NP_001394836.1:p.Ala1382Gly
  • NP_001394837.1:p.Ala1382Gly
  • NP_001394838.1:p.Ala1382Gly
  • NP_001394839.1:p.Ala1382Gly
  • NP_001394844.1:p.Ala1381Gly
  • NP_001394848.1:p.Ala1412Gly
  • NP_001394849.1:p.Ala1365Gly
  • NP_001394850.1:p.Ala1365Gly
  • NP_001394851.1:p.Ala1365Gly
  • NP_001394852.1:p.Ala1365Gly
  • NP_001394853.1:p.Ala1365Gly
  • NP_001394854.1:p.Ala1365Gly
  • NP_001394855.1:p.Ala1365Gly
  • NP_001394859.1:p.Ala1364Gly
  • NP_001394860.1:p.Ala1364Gly
  • NP_001394861.1:p.Ala1364Gly
  • NP_001394862.1:p.Ala1364Gly
  • NP_001394863.1:p.Ala1363Gly
  • NP_001394866.1:p.Ala1412Gly
  • NP_001394867.1:p.Ala1412Gly
  • NP_001394869.1:p.Ala1411Gly
  • NP_001394871.1:p.Ala1406Gly
  • NP_001394872.1:p.Ala1405Gly
  • NP_001394875.1:p.Ala1342Gly
  • NP_001394876.1:p.Ala1342Gly
  • NP_001394877.1:p.Ala1342Gly
  • NP_001394878.1:p.Ala1342Gly
  • NP_001394881.1:p.Ala1341Gly
  • NP_001394882.1:p.Ala1341Gly
  • NP_001394883.1:p.Ala1341Gly
  • NP_001394884.1:p.Ala1341Gly
  • NP_001394885.1:p.Ala1340Gly
  • NP_001394888.1:p.Ala1326Gly
  • NP_001394891.1:p.Ala1325Gly
  • NP_001394894.1:p.Ala1284Gly
  • NP_001394895.1:p.Ala1157Gly
  • NP_001394897.1:p.Ala585Gly
  • NP_001394898.1:p.Ala584Gly
  • NP_001394899.1:p.Ala372Gly
  • NP_001394900.1:p.Ala372Gly
  • NP_001394901.1:p.Ala371Gly
  • NP_001394902.1:p.Ala350Gly
  • NP_001394903.1:p.Ala350Gly
  • NP_001394904.1:p.Ala350Gly
  • NP_001394905.1:p.Ala350Gly
  • NP_001394906.1:p.Ala350Gly
  • NP_001394907.1:p.Ala350Gly
  • NP_001394908.1:p.Ala349Gly
  • NP_001394909.1:p.Ala349Gly
  • NP_001394910.1:p.Ala349Gly
  • NP_001394911.1:p.Ala349Gly
  • NP_001394912.1:p.Ala349Gly
  • NP_001394913.1:p.Ala349Gly
  • NP_001394914.1:p.Ala349Gly
  • NP_001394915.1:p.Ala349Gly
  • NP_001394919.1:p.Ala349Gly
  • NP_001394920.1:p.Ala349Gly
  • NP_001394921.1:p.Ala349Gly
  • NP_001395329.1:p.Ala348Gly
  • NP_001395330.1:p.Ala348Gly
  • NP_001395331.1:p.Ala348Gly
  • NP_001395335.1:p.Ala347Gly
  • NP_001395337.1:p.Ala347Gly
  • NP_001395338.1:p.Ala346Gly
  • NP_001395339.1:p.Ala325Gly
  • NP_001395340.1:p.Ala324Gly
  • NP_001395342.1:p.Ala323Gly
  • NP_001395345.1:p.Ala323Gly
  • NP_001395347.1:p.Ala311Gly
  • NP_001395348.1:p.Ala311Gly
  • NP_001395349.1:p.Ala311Gly
  • NP_001395350.1:p.Ala310Gly
  • NP_001395353.1:p.Ala310Gly
  • NP_001395354.1:p.Ala309Gly
  • NP_001395355.1:p.Ala309Gly
  • NP_001395356.1:p.Ala309Gly
  • NP_001395357.1:p.Ala309Gly
  • NP_001395358.1:p.Ala309Gly
  • NP_001395359.1:p.Ala309Gly
  • NP_001395361.1:p.Ala308Gly
  • NP_001395362.1:p.Ala308Gly
  • NP_001395363.1:p.Ala308Gly
  • NP_001395364.1:p.Ala308Gly
  • NP_001395370.1:p.Ala308Gly
  • NP_001395371.1:p.Ala308Gly
  • NP_001395372.1:p.Ala308Gly
  • NP_001395373.1:p.Ala308Gly
  • NP_001395380.1:p.Ala305Gly
  • NP_001395381.1:p.Ala303Gly
  • NP_001395382.1:p.Ala303Gly
  • NP_001395383.1:p.Ala303Gly
  • NP_001395384.1:p.Ala303Gly
  • NP_001395385.1:p.Ala303Gly
  • NP_001395386.1:p.Ala303Gly
  • NP_001395391.1:p.Ala302Gly
  • NP_001395392.1:p.Ala302Gly
  • NP_001395393.1:p.Ala302Gly
  • NP_001395394.1:p.Ala302Gly
  • NP_001395395.1:p.Ala302Gly
  • NP_001395396.1:p.Ala302Gly
  • NP_001395399.1:p.Ala301Gly
  • NP_001395401.1:p.Ala349Gly
  • NP_001395403.1:p.Ala283Gly
  • NP_001395404.1:p.Ala282Gly
  • NP_001395407.1:p.Ala280Gly
  • NP_001395408.1:p.Ala280Gly
  • NP_001395409.1:p.Ala280Gly
  • NP_001395418.1:p.Ala279Gly
  • NP_001395419.1:p.Ala279Gly
  • NP_001395420.1:p.Ala279Gly
  • NP_001395423.1:p.Ala270Gly
  • NP_001395425.1:p.Ala262Gly
  • NP_001395426.1:p.Ala262Gly
  • NP_001395427.1:p.Ala262Gly
  • NP_001395428.1:p.Ala262Gly
  • NP_001395429.1:p.Ala262Gly
  • NP_001395430.1:p.Ala262Gly
  • NP_001395431.1:p.Ala261Gly
  • NP_001395432.1:p.Ala261Gly
  • NP_001395433.1:p.Ala261Gly
  • NP_001395435.1:p.Ala241Gly
  • NP_001395436.1:p.Ala240Gly
  • NP_001395437.1:p.Ala237Gly
  • NP_001395439.1:p.Ala223Gly
  • NP_001395440.1:p.Ala222Gly
  • NP_001395441.1:p.Ala182Gly
  • NP_009225.1:p.Ala1453Gly
  • NP_009225.1:p.Ala1453Gly
  • NP_009228.2:p.Ala1406Gly
  • LRG_292t1:c.4358C>G
  • LRG_292:g.141370C>G
  • LRG_292p1:p.Ala1453Gly
  • NC_000017.10:g.41228631G>C
  • NM_007294.3:c.4358C>G
  • NR_027676.1:n.4494C>G
Protein change:
A1157G
Molecular consequence:
  • NM_001407583.1:c.4424-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407585.1:c.4424-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407590.1:c.4421-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407591.1:c.4421-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407616.1:c.4358-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407617.1:c.4358-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407618.1:c.4358-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407619.1:c.4358-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407620.1:c.4358-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407621.1:c.4358-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407622.1:c.4358-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407623.1:c.4358-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407633.1:c.4355-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407634.1:c.4355-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407635.1:c.4355-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407636.1:c.4355-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407637.1:c.4355-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407638.1:c.4355-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407639.1:c.4355-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407640.1:c.4355-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407641.1:c.4355-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407642.1:c.4355-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407644.1:c.4352-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407645.1:c.4352-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407647.1:c.4346-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407657.1:c.4280-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407658.1:c.4280-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407661.1:c.4277-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407662.1:c.4277-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407663.1:c.4277-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407677.1:c.4235-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407678.1:c.4235-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407679.1:c.4235-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407680.1:c.4235-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407681.1:c.4232-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407682.1:c.4232-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407683.1:c.4232-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407688.1:c.4232-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407689.1:c.4232-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407690.1:c.4229-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407691.1:c.4229-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407732.1:c.4217-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407733.1:c.4217-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407734.1:c.4217-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407735.1:c.4217-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407736.1:c.4217-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407737.1:c.4217-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407738.1:c.4217-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407739.1:c.4217-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407838.1:c.4214-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407839.1:c.4214-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407841.1:c.4214-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407842.1:c.4214-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407843.1:c.4214-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407844.1:c.4214-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407845.1:c.4214-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407846.1:c.4214-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407850.1:c.4214-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407851.1:c.4214-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407852.1:c.4214-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407858.1:c.4358-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407859.1:c.4358-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407861.1:c.4355-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407863.1:c.4235-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407874.1:c.4154-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407875.1:c.4154-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407900.1:c.4148-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407902.1:c.4148-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407904.1:c.4148-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407906.1:c.4148-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407916.1:c.4145-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407917.1:c.4145-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407918.1:c.4145-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407927.1:c.4094-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407928.1:c.4094-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407929.1:c.4094-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407935.1:c.4091-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407936.1:c.4091-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407939.1:c.4235-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407941.1:c.4232-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407944.1:c.4217-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407945.1:c.4217-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407950.1:c.4025-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407951.1:c.4025-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407957.1:c.4022-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407958.1:c.4022-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407960.1:c.3977-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407963.1:c.3974-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407964.1:c.4214-5376C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407967.1:c.3470-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.1049-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.1046-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.1046-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.1046-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.1046-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.1046-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.1046-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.1046-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.1043-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.971-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.971-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.971-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.932-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.932-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.929-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.926-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.926-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.926-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.926-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.926-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.923-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.923-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.923-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.923-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.923-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.908-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.908-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.908-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.908-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.905-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.905-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.1046-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.848-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.839-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.839-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.839-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.839-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.839-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.836-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.836-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.806-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.782-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.710-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.836-5376C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.838+5790C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.1049-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.1049-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007300.4:c.4424-3C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407571.1:c.4145C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.4424C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.4424C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.4421C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.4355C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.4355C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.4355C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.4355C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.4355C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.4355C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.4355C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.4355C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.4355C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.4352C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.4352C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.4352C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.4352C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.4352C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.4352C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.4346C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.4301C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.4298C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.4280C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.4280C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.4280C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.4277C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.4274C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.4274C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.4235C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.4235C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.4235C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.4235C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.4235C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.4235C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.4232C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.4232C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.4232C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.4232C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.4232C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.4232C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.4232C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.4229C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.4229C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.4229C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.4211C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.4211C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.4211C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.4211C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.4355C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.4157C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.4148C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.4148C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.4148C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.4148C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.4148C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.4148C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.4148C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.4148C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.4145C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.4145C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.4145C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.4145C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.4145C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.4145C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.4145C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.4145C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.4145C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.4145C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.4142C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.4235C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.4094C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.4094C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.4094C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.4094C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.4094C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.4094C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.4094C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.4091C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.4091C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.4091C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.4091C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.4088C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.4235C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.4235C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.4232C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.4214C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.4025C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.4025C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.4025C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.4025C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.4022C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.4022C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.4022C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.4022C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.4019C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.3977C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.3974C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.3851C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.3470C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407968.1:c.1754C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407969.1:c.1751C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407970.1:c.1115C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407971.1:c.1115C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407972.1:c.1112C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407973.1:c.1049C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407974.1:c.1049C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407975.1:c.1049C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407976.1:c.1049C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407977.1:c.1049C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407978.1:c.1049C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407979.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407980.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407981.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407982.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407983.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407984.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407985.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407986.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407990.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407991.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407992.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408400.1:c.1043C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408401.1:c.1043C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408402.1:c.1043C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408406.1:c.1040C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408408.1:c.1040C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408409.1:c.1037C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408410.1:c.974C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408411.1:c.971C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408413.1:c.968C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408416.1:c.968C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408418.1:c.932C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408419.1:c.932C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408420.1:c.932C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408421.1:c.929C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408424.1:c.929C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408425.1:c.926C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408426.1:c.926C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408427.1:c.926C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408428.1:c.926C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408429.1:c.926C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408430.1:c.926C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408432.1:c.923C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408433.1:c.923C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408434.1:c.923C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408435.1:c.923C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408441.1:c.923C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408442.1:c.923C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408443.1:c.923C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408444.1:c.923C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408451.1:c.914C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408452.1:c.908C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408453.1:c.908C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408454.1:c.908C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408455.1:c.908C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408456.1:c.908C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408457.1:c.908C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408462.1:c.905C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408463.1:c.905C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408464.1:c.905C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408465.1:c.905C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408466.1:c.905C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408467.1:c.905C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408470.1:c.902C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408472.1:c.1046C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408474.1:c.848C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408475.1:c.845C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408478.1:c.839C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408479.1:c.839C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408480.1:c.839C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408489.1:c.836C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408490.1:c.836C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408491.1:c.836C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408494.1:c.809C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408496.1:c.785C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408497.1:c.785C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408498.1:c.785C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408499.1:c.785C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408500.1:c.785C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408501.1:c.785C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408502.1:c.782C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408503.1:c.782C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408504.1:c.782C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408506.1:c.722C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408507.1:c.719C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408508.1:c.710C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408510.1:c.668C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408511.1:c.665C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408512.1:c.545C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.4358C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.4217C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002627513Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Feb 28, 2022) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV002627513.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The p.A1453G variant (also known as c.4358C>G) is located in coding exon 12 of the BRCA1 gene. The alanine at codon 1453 is replaced by glycine, an amino acid with similar properties. This change occurs in the first base pair of coding exon 12. This amino acid position is not well conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: May 1, 2024