U.S. flag

An official website of the United States government

NM_007294.4(BRCA1):c.86A>G (p.Glu29Gly) AND Hereditary cancer-predisposing syndrome

Germline classification:
Likely benign (1 submission)
Last evaluated:
Mar 22, 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:
RCV000218323.12

Allele description [Variation Report for NM_007294.4(BRCA1):c.86A>G (p.Glu29Gly)]

NM_007294.4(BRCA1):c.86A>G (p.Glu29Gly)

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.86A>G (p.Glu29Gly)
HGVS:
  • NC_000017.11:g.43115774T>C
  • NG_005905.2:g.102210A>G
  • NM_001407571.1:c.-103A>G
  • NM_001407581.1:c.86A>G
  • NM_001407582.1:c.86A>G
  • NM_001407583.1:c.86A>G
  • NM_001407585.1:c.86A>G
  • NM_001407587.1:c.86A>G
  • NM_001407590.1:c.86A>G
  • NM_001407591.1:c.86A>G
  • NM_001407593.1:c.86A>G
  • NM_001407594.1:c.86A>G
  • NM_001407596.1:c.86A>G
  • NM_001407597.1:c.86A>G
  • NM_001407598.1:c.86A>G
  • NM_001407602.1:c.86A>G
  • NM_001407603.1:c.86A>G
  • NM_001407605.1:c.86A>G
  • NM_001407610.1:c.86A>G
  • NM_001407611.1:c.86A>G
  • NM_001407612.1:c.86A>G
  • NM_001407613.1:c.86A>G
  • NM_001407614.1:c.86A>G
  • NM_001407615.1:c.86A>G
  • NM_001407616.1:c.86A>G
  • NM_001407617.1:c.86A>G
  • NM_001407618.1:c.86A>G
  • NM_001407619.1:c.86A>G
  • NM_001407620.1:c.86A>G
  • NM_001407621.1:c.86A>G
  • NM_001407622.1:c.86A>G
  • NM_001407623.1:c.86A>G
  • NM_001407624.1:c.86A>G
  • NM_001407625.1:c.86A>G
  • NM_001407626.1:c.86A>G
  • NM_001407627.1:c.86A>G
  • NM_001407628.1:c.86A>G
  • NM_001407629.1:c.86A>G
  • NM_001407630.1:c.86A>G
  • NM_001407631.1:c.86A>G
  • NM_001407632.1:c.86A>G
  • NM_001407633.1:c.86A>G
  • NM_001407634.1:c.86A>G
  • NM_001407635.1:c.86A>G
  • NM_001407636.1:c.86A>G
  • NM_001407637.1:c.86A>G
  • NM_001407638.1:c.86A>G
  • NM_001407639.1:c.86A>G
  • NM_001407640.1:c.86A>G
  • NM_001407641.1:c.86A>G
  • NM_001407642.1:c.86A>G
  • NM_001407644.1:c.86A>G
  • NM_001407645.1:c.86A>G
  • NM_001407646.1:c.86A>G
  • NM_001407647.1:c.86A>G
  • NM_001407648.1:c.86A>G
  • NM_001407649.1:c.86A>G
  • NM_001407652.1:c.86A>G
  • NM_001407653.1:c.86A>G
  • NM_001407654.1:c.86A>G
  • NM_001407655.1:c.86A>G
  • NM_001407656.1:c.86A>G
  • NM_001407657.1:c.86A>G
  • NM_001407658.1:c.86A>G
  • NM_001407659.1:c.86A>G
  • NM_001407660.1:c.86A>G
  • NM_001407661.1:c.86A>G
  • NM_001407662.1:c.86A>G
  • NM_001407663.1:c.86A>G
  • NM_001407664.1:c.86A>G
  • NM_001407665.1:c.86A>G
  • NM_001407666.1:c.86A>G
  • NM_001407667.1:c.86A>G
  • NM_001407668.1:c.86A>G
  • NM_001407669.1:c.86A>G
  • NM_001407670.1:c.86A>G
  • NM_001407671.1:c.86A>G
  • NM_001407672.1:c.86A>G
  • NM_001407673.1:c.86A>G
  • NM_001407674.1:c.86A>G
  • NM_001407675.1:c.86A>G
  • NM_001407676.1:c.86A>G
  • NM_001407677.1:c.86A>G
  • NM_001407678.1:c.86A>G
  • NM_001407679.1:c.86A>G
  • NM_001407680.1:c.86A>G
  • NM_001407681.1:c.86A>G
  • NM_001407682.1:c.86A>G
  • NM_001407683.1:c.86A>G
  • NM_001407684.1:c.86A>G
  • NM_001407685.1:c.86A>G
  • NM_001407686.1:c.86A>G
  • NM_001407687.1:c.86A>G
  • NM_001407688.1:c.86A>G
  • NM_001407689.1:c.86A>G
  • NM_001407690.1:c.86A>G
  • NM_001407691.1:c.86A>G
  • NM_001407694.1:c.-172A>G
  • NM_001407695.1:c.-176A>G
  • NM_001407696.1:c.-172A>G
  • NM_001407697.1:c.-56A>G
  • NM_001407724.1:c.-172A>G
  • NM_001407725.1:c.-56A>G
  • NM_001407727.1:c.-172A>G
  • NM_001407728.1:c.-56A>G
  • NM_001407729.1:c.-56A>G
  • NM_001407730.1:c.-56A>G
  • NM_001407731.1:c.-172A>G
  • NM_001407733.1:c.-172A>G
  • NM_001407734.1:c.-56A>G
  • NM_001407735.1:c.-56A>G
  • NM_001407737.1:c.-56A>G
  • NM_001407739.1:c.-56A>G
  • NM_001407740.1:c.-56A>G
  • NM_001407741.1:c.-56A>G
  • NM_001407743.1:c.-56A>G
  • NM_001407745.1:c.-56A>G
  • NM_001407746.1:c.-172A>G
  • NM_001407748.1:c.-56A>G
  • NM_001407749.1:c.-172A>G
  • NM_001407752.1:c.-56A>G
  • NM_001407838.1:c.-56A>G
  • NM_001407839.1:c.-56A>G
  • NM_001407841.1:c.-52A>G
  • NM_001407842.1:c.-172A>G
  • NM_001407843.1:c.-172A>G
  • NM_001407844.1:c.-56A>G
  • NM_001407846.1:c.-56A>G
  • NM_001407847.1:c.-56A>G
  • NM_001407848.1:c.-56A>G
  • NM_001407850.1:c.-56A>G
  • NM_001407851.1:c.-56A>G
  • NM_001407853.1:c.-103A>G
  • NM_001407854.1:c.86A>G
  • NM_001407858.1:c.86A>G
  • NM_001407859.1:c.86A>G
  • NM_001407860.1:c.86A>G
  • NM_001407861.1:c.86A>G
  • NM_001407862.1:c.86A>G
  • NM_001407863.1:c.86A>G
  • NM_001407874.1:c.86A>G
  • NM_001407875.1:c.86A>G
  • NM_001407879.1:c.-103A>G
  • NM_001407882.1:c.-103A>G
  • NM_001407884.1:c.-103A>G
  • NM_001407885.1:c.-103A>G
  • NM_001407886.1:c.-103A>G
  • NM_001407887.1:c.-103A>G
  • NM_001407889.1:c.-219A>G
  • NM_001407894.1:c.-103A>G
  • NM_001407895.1:c.-103A>G
  • NM_001407896.1:c.-103A>G
  • NM_001407897.1:c.-103A>G
  • NM_001407899.1:c.-103A>G
  • NM_001407900.1:c.-219A>G
  • NM_001407904.1:c.-103A>G
  • NM_001407906.1:c.-103A>G
  • NM_001407907.1:c.-103A>G
  • NM_001407908.1:c.-103A>G
  • NM_001407909.1:c.-103A>G
  • NM_001407910.1:c.-103A>G
  • NM_001407915.1:c.-103A>G
  • NM_001407916.1:c.-103A>G
  • NM_001407917.1:c.-103A>G
  • NM_001407918.1:c.-103A>G
  • NM_001407919.1:c.86A>G
  • NM_001407920.1:c.-56A>G
  • NM_001407921.1:c.-56A>G
  • NM_001407922.1:c.-56A>G
  • NM_001407923.1:c.-56A>G
  • NM_001407926.1:c.-56A>G
  • NM_001407927.1:c.-56A>G
  • NM_001407930.1:c.-172A>G
  • NM_001407933.1:c.-56A>G
  • NM_001407934.1:c.-56A>G
  • NM_001407935.1:c.-56A>G
  • NM_001407937.1:c.86A>G
  • NM_001407938.1:c.86A>G
  • NM_001407939.1:c.86A>G
  • NM_001407940.1:c.86A>G
  • NM_001407941.1:c.86A>G
  • NM_001407942.1:c.-172A>G
  • NM_001407943.1:c.-56A>G
  • NM_001407944.1:c.-56A>G
  • NM_001407946.1:c.-103A>G
  • NM_001407947.1:c.-103A>G
  • NM_001407948.1:c.-103A>G
  • NM_001407949.1:c.-103A>G
  • NM_001407950.1:c.-103A>G
  • NM_001407951.1:c.-103A>G
  • NM_001407952.1:c.-103A>G
  • NM_001407953.1:c.-103A>G
  • NM_001407954.1:c.-103A>G
  • NM_001407955.1:c.-103A>G
  • NM_001407956.1:c.-103A>G
  • NM_001407957.1:c.-103A>G
  • NM_001407958.1:c.-103A>G
  • NM_001407960.1:c.-218A>G
  • NM_001407962.1:c.-218A>G
  • NM_001407964.1:c.-56A>G
  • NM_001407965.1:c.-334A>G
  • NM_001407968.1:c.86A>G
  • NM_001407969.1:c.86A>G
  • NM_001407970.1:c.86A>G
  • NM_001407971.1:c.86A>G
  • NM_001407972.1:c.86A>G
  • NM_001407973.1:c.86A>G
  • NM_001407974.1:c.86A>G
  • NM_001407975.1:c.86A>G
  • NM_001407976.1:c.86A>G
  • NM_001407977.1:c.86A>G
  • NM_001407978.1:c.86A>G
  • NM_001407979.1:c.86A>G
  • NM_001407980.1:c.86A>G
  • NM_001407981.1:c.86A>G
  • NM_001407982.1:c.86A>G
  • NM_001407983.1:c.86A>G
  • NM_001407984.1:c.86A>G
  • NM_001407985.1:c.86A>G
  • NM_001407986.1:c.86A>G
  • NM_001407990.1:c.86A>G
  • NM_001407991.1:c.86A>G
  • NM_001407992.1:c.86A>G
  • NM_001407993.1:c.86A>G
  • NM_001408392.1:c.86A>G
  • NM_001408396.1:c.86A>G
  • NM_001408397.1:c.86A>G
  • NM_001408398.1:c.86A>G
  • NM_001408399.1:c.86A>G
  • NM_001408400.1:c.86A>G
  • NM_001408401.1:c.86A>G
  • NM_001408402.1:c.86A>G
  • NM_001408403.1:c.86A>G
  • NM_001408404.1:c.86A>G
  • NM_001408406.1:c.86A>G
  • NM_001408407.1:c.86A>G
  • NM_001408408.1:c.86A>G
  • NM_001408409.1:c.86A>G
  • NM_001408410.1:c.-56A>G
  • NM_001408411.1:c.86A>G
  • NM_001408412.1:c.86A>G
  • NM_001408413.1:c.86A>G
  • NM_001408414.1:c.86A>G
  • NM_001408415.1:c.86A>G
  • NM_001408416.1:c.86A>G
  • NM_001408418.1:c.86A>G
  • NM_001408419.1:c.86A>G
  • NM_001408420.1:c.86A>G
  • NM_001408421.1:c.86A>G
  • NM_001408422.1:c.86A>G
  • NM_001408423.1:c.86A>G
  • NM_001408424.1:c.86A>G
  • NM_001408425.1:c.86A>G
  • NM_001408426.1:c.86A>G
  • NM_001408427.1:c.86A>G
  • NM_001408428.1:c.86A>G
  • NM_001408429.1:c.86A>G
  • NM_001408430.1:c.86A>G
  • NM_001408431.1:c.86A>G
  • NM_001408432.1:c.86A>G
  • NM_001408433.1:c.86A>G
  • NM_001408434.1:c.86A>G
  • NM_001408435.1:c.86A>G
  • NM_001408436.1:c.86A>G
  • NM_001408437.1:c.86A>G
  • NM_001408438.1:c.86A>G
  • NM_001408439.1:c.86A>G
  • NM_001408440.1:c.86A>G
  • NM_001408441.1:c.86A>G
  • NM_001408442.1:c.86A>G
  • NM_001408443.1:c.86A>G
  • NM_001408444.1:c.86A>G
  • NM_001408445.1:c.86A>G
  • NM_001408446.1:c.86A>G
  • NM_001408447.1:c.86A>G
  • NM_001408448.1:c.86A>G
  • NM_001408450.1:c.86A>G
  • NM_001408452.1:c.-56A>G
  • NM_001408453.1:c.-56A>G
  • NM_001408455.1:c.-172A>G
  • NM_001408456.1:c.-172A>G
  • NM_001408458.1:c.-56A>G
  • NM_001408462.1:c.-56A>G
  • NM_001408463.1:c.-56A>G
  • NM_001408465.1:c.-176A>G
  • NM_001408466.1:c.-56A>G
  • NM_001408468.1:c.-172A>G
  • NM_001408469.1:c.-56A>G
  • NM_001408470.1:c.-56A>G
  • NM_001408472.1:c.86A>G
  • NM_001408473.1:c.86A>G
  • NM_001408474.1:c.86A>G
  • NM_001408475.1:c.86A>G
  • NM_001408476.1:c.86A>G
  • NM_001408478.1:c.-103A>G
  • NM_001408479.1:c.-103A>G
  • NM_001408480.1:c.-103A>G
  • NM_001408481.1:c.-103A>G
  • NM_001408482.1:c.-103A>G
  • NM_001408483.1:c.-103A>G
  • NM_001408484.1:c.-103A>G
  • NM_001408485.1:c.-103A>G
  • NM_001408489.1:c.-103A>G
  • NM_001408490.1:c.-103A>G
  • NM_001408491.1:c.-103A>G
  • NM_001408492.1:c.-219A>G
  • NM_001408493.1:c.-103A>G
  • NM_001408494.1:c.86A>G
  • NM_001408495.1:c.86A>G
  • NM_001408497.1:c.-56A>G
  • NM_001408499.1:c.-56A>G
  • NM_001408500.1:c.-56A>G
  • NM_001408501.1:c.-172A>G
  • NM_001408502.1:c.-103A>G
  • NM_001408503.1:c.-56A>G
  • NM_001408504.1:c.-56A>G
  • NM_001408505.1:c.-56A>G
  • NM_001408506.1:c.-103A>G
  • NM_001408507.1:c.-103A>G
  • NM_001408508.1:c.-103A>G
  • NM_001408509.1:c.-103A>G
  • NM_001408510.1:c.-218A>G
  • NM_001408512.1:c.-218A>G
  • NM_001408513.1:c.-103A>G
  • NM_001408514.1:c.-103A>G
  • NM_007294.4:c.86A>GMANE SELECT
  • NM_007297.4:c.-8+8243A>G
  • NM_007298.4:c.86A>G
  • NM_007299.4:c.86A>G
  • NM_007300.4:c.86A>G
  • NM_007304.2:c.86A>G
  • NP_001394510.1:p.Glu29Gly
  • NP_001394511.1:p.Glu29Gly
  • NP_001394512.1:p.Glu29Gly
  • NP_001394514.1:p.Glu29Gly
  • NP_001394516.1:p.Glu29Gly
  • NP_001394519.1:p.Glu29Gly
  • NP_001394520.1:p.Glu29Gly
  • NP_001394522.1:p.Glu29Gly
  • NP_001394523.1:p.Glu29Gly
  • NP_001394525.1:p.Glu29Gly
  • NP_001394526.1:p.Glu29Gly
  • NP_001394527.1:p.Glu29Gly
  • NP_001394531.1:p.Glu29Gly
  • NP_001394532.1:p.Glu29Gly
  • NP_001394534.1:p.Glu29Gly
  • NP_001394539.1:p.Glu29Gly
  • NP_001394540.1:p.Glu29Gly
  • NP_001394541.1:p.Glu29Gly
  • NP_001394542.1:p.Glu29Gly
  • NP_001394543.1:p.Glu29Gly
  • NP_001394544.1:p.Glu29Gly
  • NP_001394545.1:p.Glu29Gly
  • NP_001394546.1:p.Glu29Gly
  • NP_001394547.1:p.Glu29Gly
  • NP_001394548.1:p.Glu29Gly
  • NP_001394549.1:p.Glu29Gly
  • NP_001394550.1:p.Glu29Gly
  • NP_001394551.1:p.Glu29Gly
  • NP_001394552.1:p.Glu29Gly
  • NP_001394553.1:p.Glu29Gly
  • NP_001394554.1:p.Glu29Gly
  • NP_001394555.1:p.Glu29Gly
  • NP_001394556.1:p.Glu29Gly
  • NP_001394557.1:p.Glu29Gly
  • NP_001394558.1:p.Glu29Gly
  • NP_001394559.1:p.Glu29Gly
  • NP_001394560.1:p.Glu29Gly
  • NP_001394561.1:p.Glu29Gly
  • NP_001394562.1:p.Glu29Gly
  • NP_001394563.1:p.Glu29Gly
  • NP_001394564.1:p.Glu29Gly
  • NP_001394565.1:p.Glu29Gly
  • NP_001394566.1:p.Glu29Gly
  • NP_001394567.1:p.Glu29Gly
  • NP_001394568.1:p.Glu29Gly
  • NP_001394569.1:p.Glu29Gly
  • NP_001394570.1:p.Glu29Gly
  • NP_001394571.1:p.Glu29Gly
  • NP_001394573.1:p.Glu29Gly
  • NP_001394574.1:p.Glu29Gly
  • NP_001394575.1:p.Glu29Gly
  • NP_001394576.1:p.Glu29Gly
  • NP_001394577.1:p.Glu29Gly
  • NP_001394578.1:p.Glu29Gly
  • NP_001394581.1:p.Glu29Gly
  • NP_001394582.1:p.Glu29Gly
  • NP_001394583.1:p.Glu29Gly
  • NP_001394584.1:p.Glu29Gly
  • NP_001394585.1:p.Glu29Gly
  • NP_001394586.1:p.Glu29Gly
  • NP_001394587.1:p.Glu29Gly
  • NP_001394588.1:p.Glu29Gly
  • NP_001394589.1:p.Glu29Gly
  • NP_001394590.1:p.Glu29Gly
  • NP_001394591.1:p.Glu29Gly
  • NP_001394592.1:p.Glu29Gly
  • NP_001394593.1:p.Glu29Gly
  • NP_001394594.1:p.Glu29Gly
  • NP_001394595.1:p.Glu29Gly
  • NP_001394596.1:p.Glu29Gly
  • NP_001394597.1:p.Glu29Gly
  • NP_001394598.1:p.Glu29Gly
  • NP_001394599.1:p.Glu29Gly
  • NP_001394600.1:p.Glu29Gly
  • NP_001394601.1:p.Glu29Gly
  • NP_001394602.1:p.Glu29Gly
  • NP_001394603.1:p.Glu29Gly
  • NP_001394604.1:p.Glu29Gly
  • NP_001394605.1:p.Glu29Gly
  • NP_001394606.1:p.Glu29Gly
  • NP_001394607.1:p.Glu29Gly
  • NP_001394608.1:p.Glu29Gly
  • NP_001394609.1:p.Glu29Gly
  • NP_001394610.1:p.Glu29Gly
  • NP_001394611.1:p.Glu29Gly
  • NP_001394612.1:p.Glu29Gly
  • NP_001394613.1:p.Glu29Gly
  • NP_001394614.1:p.Glu29Gly
  • NP_001394615.1:p.Glu29Gly
  • NP_001394616.1:p.Glu29Gly
  • NP_001394617.1:p.Glu29Gly
  • NP_001394618.1:p.Glu29Gly
  • NP_001394619.1:p.Glu29Gly
  • NP_001394620.1:p.Glu29Gly
  • NP_001394783.1:p.Glu29Gly
  • NP_001394787.1:p.Glu29Gly
  • NP_001394788.1:p.Glu29Gly
  • NP_001394789.1:p.Glu29Gly
  • NP_001394790.1:p.Glu29Gly
  • NP_001394791.1:p.Glu29Gly
  • NP_001394792.1:p.Glu29Gly
  • NP_001394803.1:p.Glu29Gly
  • NP_001394804.1:p.Glu29Gly
  • NP_001394848.1:p.Glu29Gly
  • NP_001394866.1:p.Glu29Gly
  • NP_001394867.1:p.Glu29Gly
  • NP_001394868.1:p.Glu29Gly
  • NP_001394869.1:p.Glu29Gly
  • NP_001394870.1:p.Glu29Gly
  • NP_001394897.1:p.Glu29Gly
  • NP_001394898.1:p.Glu29Gly
  • NP_001394899.1:p.Glu29Gly
  • NP_001394900.1:p.Glu29Gly
  • NP_001394901.1:p.Glu29Gly
  • NP_001394902.1:p.Glu29Gly
  • NP_001394903.1:p.Glu29Gly
  • NP_001394904.1:p.Glu29Gly
  • NP_001394905.1:p.Glu29Gly
  • NP_001394906.1:p.Glu29Gly
  • NP_001394907.1:p.Glu29Gly
  • NP_001394908.1:p.Glu29Gly
  • NP_001394909.1:p.Glu29Gly
  • NP_001394910.1:p.Glu29Gly
  • NP_001394911.1:p.Glu29Gly
  • NP_001394912.1:p.Glu29Gly
  • NP_001394913.1:p.Glu29Gly
  • NP_001394914.1:p.Glu29Gly
  • NP_001394915.1:p.Glu29Gly
  • NP_001394919.1:p.Glu29Gly
  • NP_001394920.1:p.Glu29Gly
  • NP_001394921.1:p.Glu29Gly
  • NP_001394922.1:p.Glu29Gly
  • NP_001395321.1:p.Glu29Gly
  • NP_001395325.1:p.Glu29Gly
  • NP_001395326.1:p.Glu29Gly
  • NP_001395327.1:p.Glu29Gly
  • NP_001395328.1:p.Glu29Gly
  • NP_001395329.1:p.Glu29Gly
  • NP_001395330.1:p.Glu29Gly
  • NP_001395331.1:p.Glu29Gly
  • NP_001395332.1:p.Glu29Gly
  • NP_001395333.1:p.Glu29Gly
  • NP_001395335.1:p.Glu29Gly
  • NP_001395336.1:p.Glu29Gly
  • NP_001395337.1:p.Glu29Gly
  • NP_001395338.1:p.Glu29Gly
  • NP_001395340.1:p.Glu29Gly
  • NP_001395341.1:p.Glu29Gly
  • NP_001395342.1:p.Glu29Gly
  • NP_001395343.1:p.Glu29Gly
  • NP_001395344.1:p.Glu29Gly
  • NP_001395345.1:p.Glu29Gly
  • NP_001395347.1:p.Glu29Gly
  • NP_001395348.1:p.Glu29Gly
  • NP_001395349.1:p.Glu29Gly
  • NP_001395350.1:p.Glu29Gly
  • NP_001395351.1:p.Glu29Gly
  • NP_001395352.1:p.Glu29Gly
  • NP_001395353.1:p.Glu29Gly
  • NP_001395354.1:p.Glu29Gly
  • NP_001395355.1:p.Glu29Gly
  • NP_001395356.1:p.Glu29Gly
  • NP_001395357.1:p.Glu29Gly
  • NP_001395358.1:p.Glu29Gly
  • NP_001395359.1:p.Glu29Gly
  • NP_001395360.1:p.Glu29Gly
  • NP_001395361.1:p.Glu29Gly
  • NP_001395362.1:p.Glu29Gly
  • NP_001395363.1:p.Glu29Gly
  • NP_001395364.1:p.Glu29Gly
  • NP_001395365.1:p.Glu29Gly
  • NP_001395366.1:p.Glu29Gly
  • NP_001395367.1:p.Glu29Gly
  • NP_001395368.1:p.Glu29Gly
  • NP_001395369.1:p.Glu29Gly
  • NP_001395370.1:p.Glu29Gly
  • NP_001395371.1:p.Glu29Gly
  • NP_001395372.1:p.Glu29Gly
  • NP_001395373.1:p.Glu29Gly
  • NP_001395374.1:p.Glu29Gly
  • NP_001395375.1:p.Glu29Gly
  • NP_001395376.1:p.Glu29Gly
  • NP_001395377.1:p.Glu29Gly
  • NP_001395379.1:p.Glu29Gly
  • NP_001395401.1:p.Glu29Gly
  • NP_001395402.1:p.Glu29Gly
  • NP_001395403.1:p.Glu29Gly
  • NP_001395404.1:p.Glu29Gly
  • NP_001395405.1:p.Glu29Gly
  • NP_001395423.1:p.Glu29Gly
  • NP_001395424.1:p.Glu29Gly
  • NP_009225.1:p.Glu29Gly
  • NP_009225.1:p.Glu29Gly
  • NP_009229.2:p.Glu29Gly
  • NP_009229.2:p.Glu29Gly
  • NP_009230.2:p.Glu29Gly
  • NP_009231.2:p.Glu29Gly
  • NP_009235.2:p.Glu29Gly
  • LRG_292t1:c.86A>G
  • LRG_292:g.102210A>G
  • LRG_292p1:p.Glu29Gly
  • NC_000017.10:g.41267791T>C
  • NM_007294.3:c.86A>G
  • NM_007298.3:c.86A>G
  • NR_027676.2:n.288A>G
Protein change:
E29G
Links:
dbSNP: rs773841328
NCBI 1000 Genomes Browser:
rs773841328
Molecular consequence:
  • NM_007297.4:c.-8+8243A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407581.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407968.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407969.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407970.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407971.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407972.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407973.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407974.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407975.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407976.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407977.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407978.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407979.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407980.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407981.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407982.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407983.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407984.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407985.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407986.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407990.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407991.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407992.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407993.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408392.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408396.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408397.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408398.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408399.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408400.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408401.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408402.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408403.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408404.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408406.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408407.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408408.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408409.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408411.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408412.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408413.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408414.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408415.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408416.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408418.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408419.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408420.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408421.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408422.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408423.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408424.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408425.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408426.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408427.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408428.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408429.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408430.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408431.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408432.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408433.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408434.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408435.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408436.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408437.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408438.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408439.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408440.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408441.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408442.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408443.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408444.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408445.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408446.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408447.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408448.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408450.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408472.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408473.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408474.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408475.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408476.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408494.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408495.1:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007298.4:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007299.4:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007304.2:c.86A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NR_027676.2:n.288A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Functional consequence:
functionally_normal [Sequence Ontology: SO:0002219] - Comment(s)

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

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000275660Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(Mar 22, 2022) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Citation Link

Help

Summary from all submissions

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

Citations

PubMed

Accurate classification of BRCA1 variants with saturation genome editing.

Findlay GM, Daza RM, Martin B, Zhang MD, Leith AP, Gasperini M, Janizek JD, Huang X, Starita LM, Shendure J.

Nature. 2018 Oct;562(7726):217-222. doi: 10.1038/s41586-018-0461-z. Epub 2018 Sep 12.

PubMed [citation]
PMID:
30209399
PMCID:
PMC6181777

Details of each submission

From Ambry Genetics, SCV000275660.7

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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

Last Updated: Nov 10, 2024