NM_007294.4(BRCA1):c.134+16T>A AND Breast-ovarian cancer, familial, susceptibility to, 1

Germline classification:: not provided (1 submission)
Review status:: no classification provided

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:: RCV001076632.3

Allele description [Variation Report for NM_007294.4(BRCA1):c.134+16T>A]

NM_007294.4(BRCA1):c.134+16T>A

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.134+16T>A

HGVS:

NC_000017.11:g.43115710A>T
NG_005905.2:g.102274T>A
NM_001407571.1:c.-55+16T>A
NM_001407581.1:c.134+16T>A
NM_001407582.1:c.134+16T>A
NM_001407583.1:c.134+16T>A
NM_001407585.1:c.134+16T>A
NM_001407587.1:c.134+16T>A
NM_001407590.1:c.134+16T>A
NM_001407591.1:c.134+16T>A
NM_001407593.1:c.134+16T>A
NM_001407594.1:c.134+16T>A
NM_001407596.1:c.134+16T>A
NM_001407597.1:c.134+16T>A
NM_001407598.1:c.134+16T>A
NM_001407602.1:c.134+16T>A
NM_001407603.1:c.134+16T>A
NM_001407605.1:c.134+16T>A
NM_001407610.1:c.134+16T>A
NM_001407611.1:c.134+16T>A
NM_001407612.1:c.134+16T>A
NM_001407613.1:c.134+16T>A
NM_001407614.1:c.134+16T>A
NM_001407615.1:c.134+16T>A
NM_001407616.1:c.134+16T>A
NM_001407617.1:c.134+16T>A
NM_001407618.1:c.134+16T>A
NM_001407619.1:c.134+16T>A
NM_001407620.1:c.134+16T>A
NM_001407621.1:c.134+16T>A
NM_001407622.1:c.134+16T>A
NM_001407623.1:c.134+16T>A
NM_001407624.1:c.134+16T>A
NM_001407625.1:c.134+16T>A
NM_001407626.1:c.134+16T>A
NM_001407627.1:c.134+16T>A
NM_001407628.1:c.134+16T>A
NM_001407629.1:c.134+16T>A
NM_001407630.1:c.134+16T>A
NM_001407631.1:c.134+16T>A
NM_001407632.1:c.134+16T>A
NM_001407633.1:c.134+16T>A
NM_001407634.1:c.134+16T>A
NM_001407635.1:c.134+16T>A
NM_001407636.1:c.134+16T>A
NM_001407637.1:c.134+16T>A
NM_001407638.1:c.134+16T>A
NM_001407639.1:c.134+16T>A
NM_001407640.1:c.134+16T>A
NM_001407641.1:c.134+16T>A
NM_001407642.1:c.134+16T>A
NM_001407644.1:c.134+16T>A
NM_001407645.1:c.134+16T>A
NM_001407646.1:c.134+16T>A
NM_001407647.1:c.134+16T>A
NM_001407648.1:c.134+16T>A
NM_001407649.1:c.134+16T>A
NM_001407652.1:c.134+16T>A
NM_001407653.1:c.134+16T>A
NM_001407654.1:c.134+16T>A
NM_001407655.1:c.134+16T>A
NM_001407656.1:c.134+16T>A
NM_001407657.1:c.134+16T>A
NM_001407658.1:c.134+16T>A
NM_001407659.1:c.134+16T>A
NM_001407660.1:c.134+16T>A
NM_001407661.1:c.134+16T>A
NM_001407662.1:c.134+16T>A
NM_001407663.1:c.134+16T>A
NM_001407664.1:c.134+16T>A
NM_001407665.1:c.134+16T>A
NM_001407666.1:c.134+16T>A
NM_001407667.1:c.134+16T>A
NM_001407668.1:c.134+16T>A
NM_001407669.1:c.134+16T>A
NM_001407670.1:c.134+16T>A
NM_001407671.1:c.134+16T>A
NM_001407672.1:c.134+16T>A
NM_001407673.1:c.134+16T>A
NM_001407674.1:c.134+16T>A
NM_001407675.1:c.134+16T>A
NM_001407676.1:c.134+16T>A
NM_001407677.1:c.134+16T>A
NM_001407678.1:c.134+16T>A
NM_001407679.1:c.134+16T>A
NM_001407680.1:c.134+16T>A
NM_001407681.1:c.134+16T>A
NM_001407682.1:c.134+16T>A
NM_001407683.1:c.134+16T>A
NM_001407684.1:c.134+16T>A
NM_001407685.1:c.134+16T>A
NM_001407686.1:c.134+16T>A
NM_001407687.1:c.134+16T>A
NM_001407688.1:c.134+16T>A
NM_001407689.1:c.134+16T>A
NM_001407690.1:c.134+16T>A
NM_001407691.1:c.134+16T>A
NM_001407692.1:c.-7-9177T>A
NM_001407694.1:c.-124+16T>A
NM_001407695.1:c.-128+16T>A
NM_001407696.1:c.-124+16T>A
NM_001407697.1:c.-8+16T>A
NM_001407698.1:c.-8+8307T>A
NM_001407724.1:c.-124+16T>A
NM_001407725.1:c.-8+16T>A
NM_001407726.1:c.-8+5848T>A
NM_001407727.1:c.-124+16T>A
NM_001407728.1:c.-8+16T>A
NM_001407729.1:c.-8+16T>A
NM_001407730.1:c.-8+16T>A
NM_001407731.1:c.-124+16T>A
NM_001407732.1:c.-8+8307T>A
NM_001407733.1:c.-124+16T>A
NM_001407734.1:c.-8+16T>A
NM_001407735.1:c.-8+16T>A
NM_001407736.1:c.-8+8307T>A
NM_001407737.1:c.-8+16T>A
NM_001407738.1:c.-8+8307T>A
NM_001407739.1:c.-8+16T>A
NM_001407740.1:c.-8+16T>A
NM_001407741.1:c.-8+16T>A
NM_001407742.1:c.-8+8307T>A
NM_001407743.1:c.-8+16T>A
NM_001407744.1:c.-8+8307T>A
NM_001407745.1:c.-8+16T>A
NM_001407746.1:c.-124+16T>A
NM_001407747.1:c.-7-9177T>A
NM_001407748.1:c.-8+16T>A
NM_001407749.1:c.-124+16T>A
NM_001407750.1:c.-8+8307T>A
NM_001407751.1:c.-8+5848T>A
NM_001407752.1:c.-8+16T>A
NM_001407838.1:c.-8+16T>A
NM_001407839.1:c.-8+16T>A
NM_001407841.1:c.-8+20T>A
NM_001407842.1:c.-124+16T>A
NM_001407843.1:c.-124+16T>A
NM_001407844.1:c.-8+16T>A
NM_001407845.1:c.-8+8307T>A
NM_001407846.1:c.-8+16T>A
NM_001407847.1:c.-8+16T>A
NM_001407848.1:c.-8+16T>A
NM_001407849.1:c.-8+8307T>A
NM_001407850.1:c.-8+16T>A
NM_001407851.1:c.-8+16T>A
NM_001407852.1:c.-8+8307T>A
NM_001407853.1:c.-55+16T>A
NM_001407854.1:c.134+16T>A
NM_001407858.1:c.134+16T>A
NM_001407859.1:c.134+16T>A
NM_001407860.1:c.134+16T>A
NM_001407861.1:c.134+16T>A
NM_001407862.1:c.134+16T>A
NM_001407863.1:c.134+16T>A
NM_001407874.1:c.134+16T>A
NM_001407875.1:c.134+16T>A
NM_001407879.1:c.-55+16T>A
NM_001407881.1:c.-55+8307T>A
NM_001407882.1:c.-55+16T>A
NM_001407884.1:c.-55+16T>A
NM_001407885.1:c.-55+16T>A
NM_001407886.1:c.-55+16T>A
NM_001407887.1:c.-55+16T>A
NM_001407889.1:c.-171+16T>A
NM_001407894.1:c.-55+16T>A
NM_001407895.1:c.-55+16T>A
NM_001407896.1:c.-55+16T>A
NM_001407897.1:c.-55+16T>A
NM_001407898.1:c.-55+8307T>A
NM_001407899.1:c.-55+16T>A
NM_001407900.1:c.-171+16T>A
NM_001407902.1:c.-55+8307T>A
NM_001407904.1:c.-55+16T>A
NM_001407906.1:c.-55+16T>A
NM_001407907.1:c.-55+16T>A
NM_001407908.1:c.-55+16T>A
NM_001407909.1:c.-55+16T>A
NM_001407910.1:c.-55+16T>A
NM_001407915.1:c.-55+16T>A
NM_001407916.1:c.-55+16T>A
NM_001407917.1:c.-55+16T>A
NM_001407918.1:c.-55+16T>A
NM_001407919.1:c.134+16T>A
NM_001407920.1:c.-8+16T>A
NM_001407921.1:c.-8+16T>A
NM_001407922.1:c.-8+16T>A
NM_001407923.1:c.-8+16T>A
NM_001407924.1:c.-8+8307T>A
NM_001407925.1:c.-8+8307T>A
NM_001407926.1:c.-8+16T>A
NM_001407927.1:c.-8+16T>A
NM_001407928.1:c.-8+8307T>A
NM_001407929.1:c.-8+8307T>A
NM_001407930.1:c.-124+16T>A
NM_001407931.1:c.-7-9177T>A
NM_001407932.1:c.-8+8307T>A
NM_001407933.1:c.-8+16T>A
NM_001407934.1:c.-8+16T>A
NM_001407935.1:c.-8+16T>A
NM_001407936.1:c.-8+8307T>A
NM_001407937.1:c.134+16T>A
NM_001407938.1:c.134+16T>A
NM_001407939.1:c.134+16T>A
NM_001407940.1:c.134+16T>A
NM_001407941.1:c.134+16T>A
NM_001407942.1:c.-124+16T>A
NM_001407943.1:c.-8+16T>A
NM_001407944.1:c.-8+16T>A
NM_001407945.1:c.-8+8307T>A
NM_001407946.1:c.-55+16T>A
NM_001407947.1:c.-55+16T>A
NM_001407948.1:c.-55+16T>A
NM_001407949.1:c.-55+16T>A
NM_001407950.1:c.-55+16T>A
NM_001407951.1:c.-55+16T>A
NM_001407952.1:c.-55+16T>A
NM_001407953.1:c.-55+16T>A
NM_001407954.1:c.-55+16T>A
NM_001407955.1:c.-55+16T>A
NM_001407956.1:c.-55+16T>A
NM_001407957.1:c.-55+16T>A
NM_001407958.1:c.-55+16T>A
NM_001407959.1:c.-170+9567T>A
NM_001407960.1:c.-170+16T>A
NM_001407962.1:c.-170+16T>A
NM_001407963.1:c.-170+9561T>A
NM_001407964.1:c.-8+16T>A
NM_001407965.1:c.-286+16T>A
NM_001407966.1:c.-219+9561T>A
NM_001407967.1:c.-219+9567T>A
NM_001407968.1:c.134+16T>A
NM_001407969.1:c.134+16T>A
NM_001407970.1:c.134+16T>A
NM_001407971.1:c.134+16T>A
NM_001407972.1:c.134+16T>A
NM_001407973.1:c.134+16T>A
NM_001407974.1:c.134+16T>A
NM_001407975.1:c.134+16T>A
NM_001407976.1:c.134+16T>A
NM_001407977.1:c.134+16T>A
NM_001407978.1:c.134+16T>A
NM_001407979.1:c.134+16T>A
NM_001407980.1:c.134+16T>A
NM_001407981.1:c.134+16T>A
NM_001407982.1:c.134+16T>A
NM_001407983.1:c.134+16T>A
NM_001407984.1:c.134+16T>A
NM_001407985.1:c.134+16T>A
NM_001407986.1:c.134+16T>A
NM_001407990.1:c.134+16T>A
NM_001407991.1:c.134+16T>A
NM_001407992.1:c.134+16T>A
NM_001407993.1:c.134+16T>A
NM_001408392.1:c.134+16T>A
NM_001408396.1:c.134+16T>A
NM_001408397.1:c.134+16T>A
NM_001408398.1:c.134+16T>A
NM_001408399.1:c.134+16T>A
NM_001408400.1:c.134+16T>A
NM_001408401.1:c.134+16T>A
NM_001408402.1:c.134+16T>A
NM_001408403.1:c.134+16T>A
NM_001408404.1:c.134+16T>A
NM_001408406.1:c.134+16T>A
NM_001408407.1:c.134+16T>A
NM_001408408.1:c.134+16T>A
NM_001408409.1:c.134+16T>A
NM_001408410.1:c.-8+16T>A
NM_001408411.1:c.134+16T>A
NM_001408412.1:c.134+16T>A
NM_001408413.1:c.134+16T>A
NM_001408414.1:c.134+16T>A
NM_001408415.1:c.134+16T>A
NM_001408416.1:c.134+16T>A
NM_001408418.1:c.134+16T>A
NM_001408419.1:c.134+16T>A
NM_001408420.1:c.134+16T>A
NM_001408421.1:c.134+16T>A
NM_001408422.1:c.134+16T>A
NM_001408423.1:c.134+16T>A
NM_001408424.1:c.134+16T>A
NM_001408425.1:c.134+16T>A
NM_001408426.1:c.134+16T>A
NM_001408427.1:c.134+16T>A
NM_001408428.1:c.134+16T>A
NM_001408429.1:c.134+16T>A
NM_001408430.1:c.134+16T>A
NM_001408431.1:c.134+16T>A
NM_001408432.1:c.134+16T>A
NM_001408433.1:c.134+16T>A
NM_001408434.1:c.134+16T>A
NM_001408435.1:c.134+16T>A
NM_001408436.1:c.134+16T>A
NM_001408437.1:c.134+16T>A
NM_001408438.1:c.134+16T>A
NM_001408439.1:c.134+16T>A
NM_001408440.1:c.134+16T>A
NM_001408441.1:c.134+16T>A
NM_001408442.1:c.134+16T>A
NM_001408443.1:c.134+16T>A
NM_001408444.1:c.134+16T>A
NM_001408445.1:c.134+16T>A
NM_001408446.1:c.134+16T>A
NM_001408447.1:c.134+16T>A
NM_001408448.1:c.134+16T>A
NM_001408450.1:c.134+16T>A
NM_001408451.1:c.80+8307T>A
NM_001408452.1:c.-8+16T>A
NM_001408453.1:c.-8+16T>A
NM_001408454.1:c.-8+8307T>A
NM_001408455.1:c.-124+16T>A
NM_001408456.1:c.-124+16T>A
NM_001408457.1:c.-7-9177T>A
NM_001408458.1:c.-8+16T>A
NM_001408459.1:c.-8+8307T>A
NM_001408460.1:c.-8+8307T>A
NM_001408461.1:c.-8+8307T>A
NM_001408462.1:c.-8+16T>A
NM_001408463.1:c.-8+16T>A
NM_001408464.1:c.-8+8307T>A
NM_001408465.1:c.-128+16T>A
NM_001408466.1:c.-8+16T>A
NM_001408467.1:c.-8+8307T>A
NM_001408468.1:c.-124+16T>A
NM_001408469.1:c.-8+16T>A
NM_001408470.1:c.-8+16T>A
NM_001408472.1:c.134+16T>A
NM_001408473.1:c.134+16T>A
NM_001408474.1:c.134+16T>A
NM_001408475.1:c.134+16T>A
NM_001408476.1:c.134+16T>A
NM_001408478.1:c.-55+16T>A
NM_001408479.1:c.-55+16T>A
NM_001408480.1:c.-55+16T>A
NM_001408481.1:c.-55+16T>A
NM_001408482.1:c.-55+16T>A
NM_001408483.1:c.-55+16T>A
NM_001408484.1:c.-55+16T>A
NM_001408485.1:c.-55+16T>A
NM_001408489.1:c.-55+16T>A
NM_001408490.1:c.-55+16T>A
NM_001408491.1:c.-55+16T>A
NM_001408492.1:c.-171+16T>A
NM_001408493.1:c.-55+16T>A
NM_001408494.1:c.134+16T>A
NM_001408495.1:c.134+16T>A
NM_001408496.1:c.-8+8307T>A
NM_001408497.1:c.-8+16T>A
NM_001408498.1:c.-8+8307T>A
NM_001408499.1:c.-8+16T>A
NM_001408500.1:c.-8+16T>A
NM_001408501.1:c.-124+16T>A
NM_001408502.1:c.-55+16T>A
NM_001408503.1:c.-8+16T>A
NM_001408504.1:c.-8+16T>A
NM_001408505.1:c.-8+16T>A
NM_001408506.1:c.-55+16T>A
NM_001408507.1:c.-55+16T>A
NM_001408508.1:c.-55+16T>A
NM_001408509.1:c.-55+16T>A
NM_001408510.1:c.-170+16T>A
NM_001408511.1:c.-7-9177T>A
NM_001408512.1:c.-170+16T>A
NM_001408513.1:c.-55+16T>A
NM_001408514.1:c.-55+16T>A
NM_007294.4:c.134+16T>AMANE SELECT
NM_007297.4:c.-8+8307T>A
NM_007298.4:c.134+16T>A
NM_007299.4:c.134+16T>A
NM_007300.4:c.134+16T>A
LRG_292t1:c.134+16T>A
LRG_292:g.102274T>A
NC_000017.10:g.41267727A>T
NM_007294.3:c.134+16T>A

Links:

dbSNP: rs2055238665

NCBI 1000 Genomes Browser:

rs2055238665

Molecular consequence:

NM_001407571.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407581.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407582.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407583.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407585.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407587.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407590.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407591.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407593.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407594.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407596.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407597.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407598.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407602.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407603.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407605.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407610.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407611.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407612.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407613.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407614.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407615.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407616.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407617.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407618.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407619.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407620.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407621.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407622.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407623.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407624.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407625.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407626.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407627.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407628.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407629.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407630.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407631.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407632.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407633.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407634.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407635.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407636.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407637.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407638.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407639.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407640.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407641.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407642.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407644.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407645.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407646.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407647.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407648.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407649.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407652.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407653.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407654.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407655.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407656.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407657.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407658.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407659.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407660.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407661.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407662.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407663.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407664.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407665.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407666.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407667.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407668.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407669.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407670.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407671.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407672.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407673.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407674.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407675.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407676.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407677.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407678.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407679.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407680.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407681.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407682.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407683.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407684.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407685.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407686.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407687.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407688.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407689.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407690.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407691.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407692.1:c.-7-9177T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407694.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407695.1:c.-128+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407696.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407697.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407698.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407724.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407725.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407726.1:c.-8+5848T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407727.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407728.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407729.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407730.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407731.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407732.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407733.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407734.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407735.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407736.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407737.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407738.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407739.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407740.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407741.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407742.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407743.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407744.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407745.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407746.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407747.1:c.-7-9177T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407748.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407749.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407750.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407751.1:c.-8+5848T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407752.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407838.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407839.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407841.1:c.-8+20T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407842.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407843.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407844.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407845.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407846.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407847.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407848.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407849.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407850.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407851.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407852.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407853.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407854.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407858.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407859.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407860.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407861.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407862.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407863.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407874.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407875.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407879.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407881.1:c.-55+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407882.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407884.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407885.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407886.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407887.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407889.1:c.-171+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407894.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407895.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407896.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407897.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407898.1:c.-55+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407899.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407900.1:c.-171+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407902.1:c.-55+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407904.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407906.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407907.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407908.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407909.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407910.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407915.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407916.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407917.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407918.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407919.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407920.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407921.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407922.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407923.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407924.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407925.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407926.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407927.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407928.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407929.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407930.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407931.1:c.-7-9177T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407932.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407933.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407934.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407935.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407936.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407937.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407938.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407939.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407940.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407941.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407942.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407943.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407944.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407945.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407946.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407947.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407948.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407949.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407950.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407951.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407952.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407953.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407954.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407955.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407956.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407957.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407958.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407959.1:c.-170+9567T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407960.1:c.-170+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407962.1:c.-170+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407963.1:c.-170+9561T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407964.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407965.1:c.-286+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407966.1:c.-219+9561T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407967.1:c.-219+9567T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407968.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407969.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407970.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407971.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407972.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407973.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407974.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407975.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407976.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407977.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407978.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407979.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407980.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407981.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407982.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407983.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407984.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407985.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407986.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407990.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407991.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407992.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001407993.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408392.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408396.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408397.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408398.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408399.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408400.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408401.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408402.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408403.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408404.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408406.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408407.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408408.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408409.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408410.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408411.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408412.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408413.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408414.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408415.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408416.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408418.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408419.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408420.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408421.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408422.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408423.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408424.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408425.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408426.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408427.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408428.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408429.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408430.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408431.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408432.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408433.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408434.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408435.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408436.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408437.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408438.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408439.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408440.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408441.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408442.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408443.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408444.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408445.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408446.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408447.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408448.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408450.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408451.1:c.80+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408452.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408453.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408454.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408455.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408456.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408457.1:c.-7-9177T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408458.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408459.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408460.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408461.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408462.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408463.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408464.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408465.1:c.-128+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408466.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408467.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408468.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408469.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408470.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408472.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408473.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408474.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408475.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408476.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408478.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408479.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408480.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408481.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408482.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408483.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408484.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408485.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408489.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408490.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408491.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408492.1:c.-171+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408493.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408494.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408495.1:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408496.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408497.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408498.1:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408499.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408500.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408501.1:c.-124+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408502.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408503.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408504.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408505.1:c.-8+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408506.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408507.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408508.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408509.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408510.1:c.-170+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408511.1:c.-7-9177T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408512.1:c.-170+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408513.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001408514.1:c.-55+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_007294.4:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_007297.4:c.-8+8307T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_007298.4:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_007299.4:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]
NM_007300.4:c.134+16T>A - intron variant - [Sequence Ontology: SO:0001627]

Functional consequence:

functionally_normal [Sequence Ontology: SO:0002219] - Comment(s)

Condition(s)

Name:: Breast-ovarian cancer, familial, susceptibility to, 1 (BROVCA1)
Synonyms:: OVARIAN CANCER, SUSCEPTIBILITY TO; Breast cancer, familial 1
Identifiers:: MONDO: MONDO:0011450; MedGen: C2676676; Orphanet: 145; OMIM: 604370

Recent activity

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CBWN6093.b1 NICHD_XGC_tropTe1 Xenopus tropicalis cDNA clone IMAGE:8858030 5', mR...
CBWN6093.b1 NICHD_XGC_tropTe1 Xenopus tropicalis cDNA clone IMAGE:8858030 5', mRNA sequence
gi|133787240|gnl|dbEST|45216844|gb| 884.1|

Nucleotide
JGI_CAAO4757.rev NIH_XGC_tropTe5 Xenopus tropicalis cDNA clone CAAO4757 3', mRNA...
JGI_CAAO4757.rev NIH_XGC_tropTe5 Xenopus tropicalis cDNA clone CAAO4757 3', mRNA sequence
gi|71937825|gnl|dbEST|30599191|gb|C 32.2|

Nucleotide
AL851473 XGC-egg Xenopus tropicalis cDNA clone TEgg013j16 5', mRNA sequence
AL851473 XGC-egg Xenopus tropicalis cDNA clone TEgg013j16 5', mRNA sequence
gi|38562472|gnl|dbEST|20575813|emb| 473.2|

Nucleotide
AL899181 XGC-egg Xenopus tropicalis cDNA clone TEgg020n03 3', mRNA sequence
AL899181 XGC-egg Xenopus tropicalis cDNA clone TEgg020n03 3', mRNA sequence
gi|38698324|gnl|dbEST|20721662|emb| 181.2|

Nucleotide
JGI_CABE5672.fwd NIH_XGC_tropOva1 Xenopus tropicalis cDNA clone IMAGE:7824244 5'...
JGI_CABE5672.fwd NIH_XGC_tropOva1 Xenopus tropicalis cDNA clone IMAGE:7824244 5', mRNA sequence
gi|59763173|gnl|dbEST|27819848|gb|D 27.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001242420	Brotman Baty Institute, University of Washington	no classification provided	not provided	not applicable	in vitro	PubMed (1) [See all records that cite this PMID] Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001242420

Brotman Baty Institute, University of Washington

no classification provided

not provided

not applicable

in vitro

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

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	not applicable	not applicable	not provided	not provided	not provided	not provided	not provided	in vitro

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 Brotman Baty Institute, University of Washington, SCV001242420.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	in vitro	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	not applicable	not applicable	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Oct 8, 2024

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