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NM_007294.4(BRCA1):c.81-17C>G AND not provided

Germline classification:
Likely benign (2 submissions)
Last evaluated:
Jun 12, 2017
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:
RCV000589921.10

Allele description [Variation Report for NM_007294.4(BRCA1):c.81-17C>G]

NM_007294.4(BRCA1):c.81-17C>G

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.81-17C>G
HGVS:
  • NC_000017.11:g.43115796G>C
  • NG_005905.2:g.102188C>G
  • NM_001407571.1:c.-108-17C>G
  • NM_001407581.1:c.81-17C>G
  • NM_001407582.1:c.81-17C>G
  • NM_001407583.1:c.81-17C>G
  • NM_001407585.1:c.81-17C>G
  • NM_001407587.1:c.81-17C>G
  • NM_001407590.1:c.81-17C>G
  • NM_001407591.1:c.81-17C>G
  • NM_001407593.1:c.81-17C>G
  • NM_001407594.1:c.81-17C>G
  • NM_001407596.1:c.81-17C>G
  • NM_001407597.1:c.81-17C>G
  • NM_001407598.1:c.81-17C>G
  • NM_001407602.1:c.81-17C>G
  • NM_001407603.1:c.81-17C>G
  • NM_001407605.1:c.81-17C>G
  • NM_001407610.1:c.81-17C>G
  • NM_001407611.1:c.81-17C>G
  • NM_001407612.1:c.81-17C>G
  • NM_001407613.1:c.81-17C>G
  • NM_001407614.1:c.81-17C>G
  • NM_001407615.1:c.81-17C>G
  • NM_001407616.1:c.81-17C>G
  • NM_001407617.1:c.81-17C>G
  • NM_001407618.1:c.81-17C>G
  • NM_001407619.1:c.81-17C>G
  • NM_001407620.1:c.81-17C>G
  • NM_001407621.1:c.81-17C>G
  • NM_001407622.1:c.81-17C>G
  • NM_001407623.1:c.81-17C>G
  • NM_001407624.1:c.81-17C>G
  • NM_001407625.1:c.81-17C>G
  • NM_001407626.1:c.81-17C>G
  • NM_001407627.1:c.81-17C>G
  • NM_001407628.1:c.81-17C>G
  • NM_001407629.1:c.81-17C>G
  • NM_001407630.1:c.81-17C>G
  • NM_001407631.1:c.81-17C>G
  • NM_001407632.1:c.81-17C>G
  • NM_001407633.1:c.81-17C>G
  • NM_001407634.1:c.81-17C>G
  • NM_001407635.1:c.81-17C>G
  • NM_001407636.1:c.81-17C>G
  • NM_001407637.1:c.81-17C>G
  • NM_001407638.1:c.81-17C>G
  • NM_001407639.1:c.81-17C>G
  • NM_001407640.1:c.81-17C>G
  • NM_001407641.1:c.81-17C>G
  • NM_001407642.1:c.81-17C>G
  • NM_001407644.1:c.81-17C>G
  • NM_001407645.1:c.81-17C>G
  • NM_001407646.1:c.81-17C>G
  • NM_001407647.1:c.81-17C>G
  • NM_001407648.1:c.81-17C>G
  • NM_001407649.1:c.81-17C>G
  • NM_001407652.1:c.81-17C>G
  • NM_001407653.1:c.81-17C>G
  • NM_001407654.1:c.81-17C>G
  • NM_001407655.1:c.81-17C>G
  • NM_001407656.1:c.81-17C>G
  • NM_001407657.1:c.81-17C>G
  • NM_001407658.1:c.81-17C>G
  • NM_001407659.1:c.81-17C>G
  • NM_001407660.1:c.81-17C>G
  • NM_001407661.1:c.81-17C>G
  • NM_001407662.1:c.81-17C>G
  • NM_001407663.1:c.81-17C>G
  • NM_001407664.1:c.81-17C>G
  • NM_001407665.1:c.81-17C>G
  • NM_001407666.1:c.81-17C>G
  • NM_001407667.1:c.81-17C>G
  • NM_001407668.1:c.81-17C>G
  • NM_001407669.1:c.81-17C>G
  • NM_001407670.1:c.81-17C>G
  • NM_001407671.1:c.81-17C>G
  • NM_001407672.1:c.81-17C>G
  • NM_001407673.1:c.81-17C>G
  • NM_001407674.1:c.81-17C>G
  • NM_001407675.1:c.81-17C>G
  • NM_001407676.1:c.81-17C>G
  • NM_001407677.1:c.81-17C>G
  • NM_001407678.1:c.81-17C>G
  • NM_001407679.1:c.81-17C>G
  • NM_001407680.1:c.81-17C>G
  • NM_001407681.1:c.81-17C>G
  • NM_001407682.1:c.81-17C>G
  • NM_001407683.1:c.81-17C>G
  • NM_001407684.1:c.81-17C>G
  • NM_001407685.1:c.81-17C>G
  • NM_001407686.1:c.81-17C>G
  • NM_001407687.1:c.81-17C>G
  • NM_001407688.1:c.81-17C>G
  • NM_001407689.1:c.81-17C>G
  • NM_001407690.1:c.81-17C>G
  • NM_001407691.1:c.81-17C>G
  • NM_001407692.1:c.-7-9263C>G
  • NM_001407694.1:c.-177-17C>G
  • NM_001407695.1:c.-181-17C>G
  • NM_001407696.1:c.-177-17C>G
  • NM_001407697.1:c.-61-17C>G
  • NM_001407698.1:c.-8+8221C>G
  • NM_001407724.1:c.-177-17C>G
  • NM_001407725.1:c.-61-17C>G
  • NM_001407726.1:c.-8+5762C>G
  • NM_001407727.1:c.-177-17C>G
  • NM_001407728.1:c.-61-17C>G
  • NM_001407729.1:c.-61-17C>G
  • NM_001407730.1:c.-61-17C>G
  • NM_001407731.1:c.-177-17C>G
  • NM_001407732.1:c.-8+8221C>G
  • NM_001407733.1:c.-177-17C>G
  • NM_001407734.1:c.-61-17C>G
  • NM_001407735.1:c.-61-17C>G
  • NM_001407736.1:c.-8+8221C>G
  • NM_001407737.1:c.-61-17C>G
  • NM_001407738.1:c.-8+8221C>G
  • NM_001407739.1:c.-61-17C>G
  • NM_001407740.1:c.-61-17C>G
  • NM_001407741.1:c.-61-17C>G
  • NM_001407742.1:c.-8+8221C>G
  • NM_001407743.1:c.-61-17C>G
  • NM_001407744.1:c.-8+8221C>G
  • NM_001407745.1:c.-61-17C>G
  • NM_001407746.1:c.-177-17C>G
  • NM_001407747.1:c.-7-9263C>G
  • NM_001407748.1:c.-61-17C>G
  • NM_001407749.1:c.-177-17C>G
  • NM_001407750.1:c.-8+8221C>G
  • NM_001407751.1:c.-8+5762C>G
  • NM_001407752.1:c.-61-17C>G
  • NM_001407838.1:c.-61-17C>G
  • NM_001407839.1:c.-61-17C>G
  • NM_001407841.1:c.-57-17C>G
  • NM_001407842.1:c.-177-17C>G
  • NM_001407843.1:c.-177-17C>G
  • NM_001407844.1:c.-61-17C>G
  • NM_001407845.1:c.-8+8221C>G
  • NM_001407846.1:c.-61-17C>G
  • NM_001407847.1:c.-61-17C>G
  • NM_001407848.1:c.-61-17C>G
  • NM_001407849.1:c.-8+8221C>G
  • NM_001407850.1:c.-61-17C>G
  • NM_001407851.1:c.-61-17C>G
  • NM_001407852.1:c.-8+8221C>G
  • NM_001407853.1:c.-108-17C>G
  • NM_001407854.1:c.81-17C>G
  • NM_001407858.1:c.81-17C>G
  • NM_001407859.1:c.81-17C>G
  • NM_001407860.1:c.81-17C>G
  • NM_001407861.1:c.81-17C>G
  • NM_001407862.1:c.81-17C>G
  • NM_001407863.1:c.81-17C>G
  • NM_001407874.1:c.81-17C>G
  • NM_001407875.1:c.81-17C>G
  • NM_001407879.1:c.-108-17C>G
  • NM_001407881.1:c.-55+8221C>G
  • NM_001407882.1:c.-108-17C>G
  • NM_001407884.1:c.-108-17C>G
  • NM_001407885.1:c.-108-17C>G
  • NM_001407886.1:c.-108-17C>G
  • NM_001407887.1:c.-108-17C>G
  • NM_001407889.1:c.-224-17C>G
  • NM_001407894.1:c.-108-17C>G
  • NM_001407895.1:c.-108-17C>G
  • NM_001407896.1:c.-108-17C>G
  • NM_001407897.1:c.-108-17C>G
  • NM_001407898.1:c.-55+8221C>G
  • NM_001407899.1:c.-108-17C>G
  • NM_001407900.1:c.-224-17C>G
  • NM_001407902.1:c.-55+8221C>G
  • NM_001407904.1:c.-108-17C>G
  • NM_001407906.1:c.-108-17C>G
  • NM_001407907.1:c.-108-17C>G
  • NM_001407908.1:c.-108-17C>G
  • NM_001407909.1:c.-108-17C>G
  • NM_001407910.1:c.-108-17C>G
  • NM_001407915.1:c.-108-17C>G
  • NM_001407916.1:c.-108-17C>G
  • NM_001407917.1:c.-108-17C>G
  • NM_001407918.1:c.-108-17C>G
  • NM_001407919.1:c.81-17C>G
  • NM_001407920.1:c.-61-17C>G
  • NM_001407921.1:c.-61-17C>G
  • NM_001407922.1:c.-61-17C>G
  • NM_001407923.1:c.-61-17C>G
  • NM_001407924.1:c.-8+8221C>G
  • NM_001407925.1:c.-8+8221C>G
  • NM_001407926.1:c.-61-17C>G
  • NM_001407927.1:c.-61-17C>G
  • NM_001407928.1:c.-8+8221C>G
  • NM_001407929.1:c.-8+8221C>G
  • NM_001407930.1:c.-177-17C>G
  • NM_001407931.1:c.-7-9263C>G
  • NM_001407932.1:c.-8+8221C>G
  • NM_001407933.1:c.-61-17C>G
  • NM_001407934.1:c.-61-17C>G
  • NM_001407935.1:c.-61-17C>G
  • NM_001407936.1:c.-8+8221C>G
  • NM_001407937.1:c.81-17C>G
  • NM_001407938.1:c.81-17C>G
  • NM_001407939.1:c.81-17C>G
  • NM_001407940.1:c.81-17C>G
  • NM_001407941.1:c.81-17C>G
  • NM_001407942.1:c.-177-17C>G
  • NM_001407943.1:c.-61-17C>G
  • NM_001407944.1:c.-61-17C>G
  • NM_001407945.1:c.-8+8221C>G
  • NM_001407946.1:c.-108-17C>G
  • NM_001407947.1:c.-108-17C>G
  • NM_001407948.1:c.-108-17C>G
  • NM_001407949.1:c.-108-17C>G
  • NM_001407950.1:c.-108-17C>G
  • NM_001407951.1:c.-108-17C>G
  • NM_001407952.1:c.-108-17C>G
  • NM_001407953.1:c.-108-17C>G
  • NM_001407954.1:c.-108-17C>G
  • NM_001407955.1:c.-108-17C>G
  • NM_001407956.1:c.-108-17C>G
  • NM_001407957.1:c.-108-17C>G
  • NM_001407958.1:c.-108-17C>G
  • NM_001407959.1:c.-170+9481C>G
  • NM_001407960.1:c.-223-17C>G
  • NM_001407962.1:c.-223-17C>G
  • NM_001407963.1:c.-170+9475C>G
  • NM_001407964.1:c.-61-17C>G
  • NM_001407965.1:c.-339-17C>G
  • NM_001407966.1:c.-219+9475C>G
  • NM_001407967.1:c.-219+9481C>G
  • NM_001407968.1:c.81-17C>G
  • NM_001407969.1:c.81-17C>G
  • NM_001407970.1:c.81-17C>G
  • NM_001407971.1:c.81-17C>G
  • NM_001407972.1:c.81-17C>G
  • NM_001407973.1:c.81-17C>G
  • NM_001407974.1:c.81-17C>G
  • NM_001407975.1:c.81-17C>G
  • NM_001407976.1:c.81-17C>G
  • NM_001407977.1:c.81-17C>G
  • NM_001407978.1:c.81-17C>G
  • NM_001407979.1:c.81-17C>G
  • NM_001407980.1:c.81-17C>G
  • NM_001407981.1:c.81-17C>G
  • NM_001407982.1:c.81-17C>G
  • NM_001407983.1:c.81-17C>G
  • NM_001407984.1:c.81-17C>G
  • NM_001407985.1:c.81-17C>G
  • NM_001407986.1:c.81-17C>G
  • NM_001407990.1:c.81-17C>G
  • NM_001407991.1:c.81-17C>G
  • NM_001407992.1:c.81-17C>G
  • NM_001407993.1:c.81-17C>G
  • NM_001408392.1:c.81-17C>G
  • NM_001408396.1:c.81-17C>G
  • NM_001408397.1:c.81-17C>G
  • NM_001408398.1:c.81-17C>G
  • NM_001408399.1:c.81-17C>G
  • NM_001408400.1:c.81-17C>G
  • NM_001408401.1:c.81-17C>G
  • NM_001408402.1:c.81-17C>G
  • NM_001408403.1:c.81-17C>G
  • NM_001408404.1:c.81-17C>G
  • NM_001408406.1:c.81-17C>G
  • NM_001408407.1:c.81-17C>G
  • NM_001408408.1:c.81-17C>G
  • NM_001408409.1:c.81-17C>G
  • NM_001408410.1:c.-61-17C>G
  • NM_001408411.1:c.81-17C>G
  • NM_001408412.1:c.81-17C>G
  • NM_001408413.1:c.81-17C>G
  • NM_001408414.1:c.81-17C>G
  • NM_001408415.1:c.81-17C>G
  • NM_001408416.1:c.81-17C>G
  • NM_001408418.1:c.81-17C>G
  • NM_001408419.1:c.81-17C>G
  • NM_001408420.1:c.81-17C>G
  • NM_001408421.1:c.81-17C>G
  • NM_001408422.1:c.81-17C>G
  • NM_001408423.1:c.81-17C>G
  • NM_001408424.1:c.81-17C>G
  • NM_001408425.1:c.81-17C>G
  • NM_001408426.1:c.81-17C>G
  • NM_001408427.1:c.81-17C>G
  • NM_001408428.1:c.81-17C>G
  • NM_001408429.1:c.81-17C>G
  • NM_001408430.1:c.81-17C>G
  • NM_001408431.1:c.81-17C>G
  • NM_001408432.1:c.81-17C>G
  • NM_001408433.1:c.81-17C>G
  • NM_001408434.1:c.81-17C>G
  • NM_001408435.1:c.81-17C>G
  • NM_001408436.1:c.81-17C>G
  • NM_001408437.1:c.81-17C>G
  • NM_001408438.1:c.81-17C>G
  • NM_001408439.1:c.81-17C>G
  • NM_001408440.1:c.81-17C>G
  • NM_001408441.1:c.81-17C>G
  • NM_001408442.1:c.81-17C>G
  • NM_001408443.1:c.81-17C>G
  • NM_001408444.1:c.81-17C>G
  • NM_001408445.1:c.81-17C>G
  • NM_001408446.1:c.81-17C>G
  • NM_001408447.1:c.81-17C>G
  • NM_001408448.1:c.81-17C>G
  • NM_001408450.1:c.81-17C>G
  • NM_001408451.1:c.80+8221C>G
  • NM_001408452.1:c.-61-17C>G
  • NM_001408453.1:c.-61-17C>G
  • NM_001408454.1:c.-8+8221C>G
  • NM_001408455.1:c.-177-17C>G
  • NM_001408456.1:c.-177-17C>G
  • NM_001408457.1:c.-7-9263C>G
  • NM_001408458.1:c.-61-17C>G
  • NM_001408459.1:c.-8+8221C>G
  • NM_001408460.1:c.-8+8221C>G
  • NM_001408461.1:c.-8+8221C>G
  • NM_001408462.1:c.-61-17C>G
  • NM_001408463.1:c.-61-17C>G
  • NM_001408464.1:c.-8+8221C>G
  • NM_001408465.1:c.-181-17C>G
  • NM_001408466.1:c.-61-17C>G
  • NM_001408467.1:c.-8+8221C>G
  • NM_001408468.1:c.-177-17C>G
  • NM_001408469.1:c.-61-17C>G
  • NM_001408470.1:c.-61-17C>G
  • NM_001408472.1:c.81-17C>G
  • NM_001408473.1:c.81-17C>G
  • NM_001408474.1:c.81-17C>G
  • NM_001408475.1:c.81-17C>G
  • NM_001408476.1:c.81-17C>G
  • NM_001408478.1:c.-108-17C>G
  • NM_001408479.1:c.-108-17C>G
  • NM_001408480.1:c.-108-17C>G
  • NM_001408481.1:c.-108-17C>G
  • NM_001408482.1:c.-108-17C>G
  • NM_001408483.1:c.-108-17C>G
  • NM_001408484.1:c.-108-17C>G
  • NM_001408485.1:c.-108-17C>G
  • NM_001408489.1:c.-108-17C>G
  • NM_001408490.1:c.-108-17C>G
  • NM_001408491.1:c.-108-17C>G
  • NM_001408492.1:c.-224-17C>G
  • NM_001408493.1:c.-108-17C>G
  • NM_001408494.1:c.81-17C>G
  • NM_001408495.1:c.81-17C>G
  • NM_001408496.1:c.-8+8221C>G
  • NM_001408497.1:c.-61-17C>G
  • NM_001408498.1:c.-8+8221C>G
  • NM_001408499.1:c.-61-17C>G
  • NM_001408500.1:c.-61-17C>G
  • NM_001408501.1:c.-177-17C>G
  • NM_001408502.1:c.-108-17C>G
  • NM_001408503.1:c.-61-17C>G
  • NM_001408504.1:c.-61-17C>G
  • NM_001408505.1:c.-61-17C>G
  • NM_001408506.1:c.-108-17C>G
  • NM_001408507.1:c.-108-17C>G
  • NM_001408508.1:c.-108-17C>G
  • NM_001408509.1:c.-108-17C>G
  • NM_001408510.1:c.-223-17C>G
  • NM_001408511.1:c.-7-9263C>G
  • NM_001408512.1:c.-223-17C>G
  • NM_001408513.1:c.-108-17C>G
  • NM_001408514.1:c.-108-17C>G
  • NM_007294.4:c.81-17C>GMANE SELECT
  • NM_007297.4:c.-8+8221C>G
  • NM_007298.4:c.81-17C>G
  • NM_007299.4:c.81-17C>G
  • NM_007300.4:c.81-17C>G
  • LRG_292t1:c.81-17C>G
  • LRG_292:g.102188C>G
  • NC_000017.10:g.41267813G>C
  • NM_007294.3:c.81-17C>G
Links:
dbSNP: rs757442952
NCBI 1000 Genomes Browser:
rs757442952
Molecular consequence:
  • NM_001407571.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407581.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407582.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407583.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407585.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407587.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407590.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407591.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407593.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407594.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407596.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407597.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407598.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407602.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407603.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407605.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407610.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407611.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407612.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407613.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407614.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407615.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407616.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407617.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407618.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407619.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407620.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407621.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407622.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407623.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407624.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407625.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407626.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407627.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407628.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407629.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407630.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407631.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407632.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407633.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407634.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407635.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407636.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407637.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407638.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407639.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407640.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407641.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407642.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407644.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407645.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407646.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407647.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407648.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407649.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407652.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407653.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407654.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407655.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407656.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407657.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407658.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407659.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407660.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407661.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407662.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407663.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407664.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407665.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407666.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407667.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407668.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407669.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407670.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407671.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407672.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407673.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407674.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407675.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407676.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407677.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407678.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407679.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407680.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407681.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407682.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407683.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407684.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407685.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407686.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407687.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407688.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407689.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407690.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407691.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407692.1:c.-7-9263C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407694.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407695.1:c.-181-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407696.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407697.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407698.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407724.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407725.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407726.1:c.-8+5762C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407727.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407728.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407729.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407730.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407731.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407732.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407733.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407734.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407735.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407736.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407737.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407738.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407739.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407740.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407741.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407742.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407743.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407744.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407745.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407746.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407747.1:c.-7-9263C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407748.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407749.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407750.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407751.1:c.-8+5762C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407752.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407838.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407839.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407841.1:c.-57-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407842.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407843.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407844.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407845.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407846.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407847.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407848.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407849.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407850.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407851.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407852.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407853.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407854.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407858.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407859.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407860.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407861.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407862.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407863.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407874.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407875.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407879.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407881.1:c.-55+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407882.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407884.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407885.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407886.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407887.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407889.1:c.-224-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407894.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407895.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407896.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407897.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407898.1:c.-55+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407899.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407900.1:c.-224-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407902.1:c.-55+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407904.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407906.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407907.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407908.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407909.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407910.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407915.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407916.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407917.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407918.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407919.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407920.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407921.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407922.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407923.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407924.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407925.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407926.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407927.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407928.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407929.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407930.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407931.1:c.-7-9263C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407932.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407933.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407934.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407935.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407936.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407937.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407938.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407939.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407940.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407941.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407942.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407943.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407944.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407945.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407946.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407947.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407948.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407949.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407950.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407951.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407952.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407953.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407954.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407955.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407956.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407957.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407958.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407959.1:c.-170+9481C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407960.1:c.-223-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407962.1:c.-223-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407963.1:c.-170+9475C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407964.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407965.1:c.-339-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407966.1:c.-219+9475C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407967.1:c.-219+9481C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407968.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407969.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407970.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.80+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.-7-9263C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.-181-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.-224-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.-177-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.-61-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.-223-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.-7-9263C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.-223-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.-108-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007294.4:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007297.4:c.-8+8221C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007300.4:c.81-17C>G - intron variant - [Sequence Ontology: SO:0001627]
Functional consequence:
functionally_normal [Sequence Ontology: SO:0002219] - Comment(s)
Observations:
1

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000591236Department of Pathology and Laboratory Medicine, Sinai Health System - The Canadian Open Genetics Repository (COGR)

See additional submitters

no assertion criteria provided
Uncertain significanceunknownclinical testing

SCV000806986PreventionGenetics, part of Exact Sciences
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely benign
(Jun 12, 2017) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownyes1not providednot providednot providednot providedclinical testing
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Department of Pathology and Laboratory Medicine, Sinai Health System - The Canadian Open Genetics Repository (COGR), SCV000591236.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providednot provided1not providednot providednot provided

From PreventionGenetics, part of Exact Sciences, SCV000806986.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 8, 2024