NM_007294.4(BRCA1):c.4987-10T>G AND Hereditary breast ovarian cancer syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 15, 2023
- Review status:
- 1 star out of maximum of 4 starscriteria provided, single submitter
- Somatic classification
of clinical impact: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno assertion criteria provided
- Somatic classification
of oncogenicity: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno assertion criteria provided
- Record status:
- current
- Accession:
- RCV003645073.2
Allele description [Variation Report for NM_007294.4(BRCA1):c.4987-10T>G]
NM_007294.4(BRCA1):c.4987-10T>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.4987-10T>G
- HGVS:
- NC_000017.11:g.43067705A>C
- NG_005905.2:g.150279T>G
- NM_001407571.1:c.4774-10T>G
- NM_001407581.1:c.5053-10T>G
- NM_001407582.1:c.5053-10T>G
- NM_001407583.1:c.5050-10T>G
- NM_001407585.1:c.5050-10T>G
- NM_001407587.1:c.5050-10T>G
- NM_001407590.1:c.5047-10T>G
- NM_001407591.1:c.5047-10T>G
- NM_001407593.1:c.4987-10T>G
- NM_001407594.1:c.4987-10T>G
- NM_001407596.1:c.4987-10T>G
- NM_001407597.1:c.4987-10T>G
- NM_001407598.1:c.4987-10T>G
- NM_001407602.1:c.4987-10T>G
- NM_001407603.1:c.4987-10T>G
- NM_001407605.1:c.4987-10T>G
- NM_001407610.1:c.4984-10T>G
- NM_001407611.1:c.4984-10T>G
- NM_001407612.1:c.4984-10T>G
- NM_001407613.1:c.4984-10T>G
- NM_001407614.1:c.4984-10T>G
- NM_001407615.1:c.4984-10T>G
- NM_001407616.1:c.4984-10T>G
- NM_001407617.1:c.4984-10T>G
- NM_001407618.1:c.4984-10T>G
- NM_001407619.1:c.4984-10T>G
- NM_001407620.1:c.4984-10T>G
- NM_001407621.1:c.4984-10T>G
- NM_001407622.1:c.4984-10T>G
- NM_001407623.1:c.4984-10T>G
- NM_001407624.1:c.4984-10T>G
- NM_001407625.1:c.4984-10T>G
- NM_001407626.1:c.4984-10T>G
- NM_001407627.1:c.4981-10T>G
- NM_001407628.1:c.4981-10T>G
- NM_001407629.1:c.4981-10T>G
- NM_001407630.1:c.4981-10T>G
- NM_001407631.1:c.4981-10T>G
- NM_001407632.1:c.4981-10T>G
- NM_001407633.1:c.4981-10T>G
- NM_001407634.1:c.4981-10T>G
- NM_001407635.1:c.4981-10T>G
- NM_001407636.1:c.4981-10T>G
- NM_001407637.1:c.4981-10T>G
- NM_001407638.1:c.4981-10T>G
- NM_001407639.1:c.4981-10T>G
- NM_001407640.1:c.4981-10T>G
- NM_001407641.1:c.4981-10T>G
- NM_001407642.1:c.4981-10T>G
- NM_001407644.1:c.4978-10T>G
- NM_001407645.1:c.4978-10T>G
- NM_001407646.1:c.4975-10T>G
- NM_001407647.1:c.4972-10T>G
- NM_001407648.1:c.4930-10T>G
- NM_001407649.1:c.4927-10T>G
- NM_001407652.1:c.4987-10T>G
- NM_001407653.1:c.4909-10T>G
- NM_001407654.1:c.4909-10T>G
- NM_001407655.1:c.4909-10T>G
- NM_001407656.1:c.4906-10T>G
- NM_001407657.1:c.4906-10T>G
- NM_001407658.1:c.4906-10T>G
- NM_001407659.1:c.4903-10T>G
- NM_001407660.1:c.4903-10T>G
- NM_001407661.1:c.4903-10T>G
- NM_001407662.1:c.4903-10T>G
- NM_001407663.1:c.4903-10T>G
- NM_001407664.1:c.4864-10T>G
- NM_001407665.1:c.4864-10T>G
- NM_001407666.1:c.4864-10T>G
- NM_001407667.1:c.4864-10T>G
- NM_001407668.1:c.4864-10T>G
- NM_001407669.1:c.4864-10T>G
- NM_001407670.1:c.4861-10T>G
- NM_001407671.1:c.4861-10T>G
- NM_001407672.1:c.4861-10T>G
- NM_001407673.1:c.4861-10T>G
- NM_001407674.1:c.4861-10T>G
- NM_001407675.1:c.4861-10T>G
- NM_001407676.1:c.4861-10T>G
- NM_001407677.1:c.4861-10T>G
- NM_001407678.1:c.4861-10T>G
- NM_001407679.1:c.4861-10T>G
- NM_001407680.1:c.4861-10T>G
- NM_001407681.1:c.4858-10T>G
- NM_001407682.1:c.4858-10T>G
- NM_001407683.1:c.4858-10T>G
- NM_001407684.1:c.4987-10T>G
- NM_001407685.1:c.4858-10T>G
- NM_001407686.1:c.4858-10T>G
- NM_001407687.1:c.4858-10T>G
- NM_001407688.1:c.4858-10T>G
- NM_001407689.1:c.4858-10T>G
- NM_001407690.1:c.4855-10T>G
- NM_001407691.1:c.4855-10T>G
- NM_001407692.1:c.4846-10T>G
- NM_001407694.1:c.4846-10T>G
- NM_001407695.1:c.4846-10T>G
- NM_001407696.1:c.4846-10T>G
- NM_001407697.1:c.4846-10T>G
- NM_001407698.1:c.4846-10T>G
- NM_001407724.1:c.4846-10T>G
- NM_001407725.1:c.4846-10T>G
- NM_001407726.1:c.4846-10T>G
- NM_001407727.1:c.4846-10T>G
- NM_001407728.1:c.4846-10T>G
- NM_001407729.1:c.4846-10T>G
- NM_001407730.1:c.4846-10T>G
- NM_001407731.1:c.4846-10T>G
- NM_001407732.1:c.4843-10T>G
- NM_001407733.1:c.4843-10T>G
- NM_001407734.1:c.4843-10T>G
- NM_001407735.1:c.4843-10T>G
- NM_001407736.1:c.4843-10T>G
- NM_001407737.1:c.4843-10T>G
- NM_001407738.1:c.4843-10T>G
- NM_001407739.1:c.4843-10T>G
- NM_001407740.1:c.4843-10T>G
- NM_001407741.1:c.4843-10T>G
- NM_001407742.1:c.4843-10T>G
- NM_001407743.1:c.4843-10T>G
- NM_001407744.1:c.4843-10T>G
- NM_001407745.1:c.4843-10T>G
- NM_001407746.1:c.4843-10T>G
- NM_001407747.1:c.4843-10T>G
- NM_001407748.1:c.4843-10T>G
- NM_001407749.1:c.4843-10T>G
- NM_001407750.1:c.4843-10T>G
- NM_001407751.1:c.4843-10T>G
- NM_001407752.1:c.4843-10T>G
- NM_001407838.1:c.4840-10T>G
- NM_001407839.1:c.4840-10T>G
- NM_001407841.1:c.4840-10T>G
- NM_001407842.1:c.4840-10T>G
- NM_001407843.1:c.4840-10T>G
- NM_001407844.1:c.4840-10T>G
- NM_001407845.1:c.4840-10T>G
- NM_001407846.1:c.4840-10T>G
- NM_001407847.1:c.4840-10T>G
- NM_001407848.1:c.4840-10T>G
- NM_001407849.1:c.4840-10T>G
- NM_001407850.1:c.4840-10T>G
- NM_001407851.1:c.4840-10T>G
- NM_001407852.1:c.4840-10T>G
- NM_001407853.1:c.4840-10T>G
- NM_001407854.1:c.4987-10T>G
- NM_001407858.1:c.4984-10T>G
- NM_001407859.1:c.4984-10T>G
- NM_001407860.1:c.4984-10T>G
- NM_001407861.1:c.4981-10T>G
- NM_001407862.1:c.4786-10T>G
- NM_001407863.1:c.4861-10T>G
- NM_001407874.1:c.4780-10T>G
- NM_001407875.1:c.4780-10T>G
- NM_001407879.1:c.4777-10T>G
- NM_001407881.1:c.4777-10T>G
- NM_001407882.1:c.4777-10T>G
- NM_001407884.1:c.4777-10T>G
- NM_001407885.1:c.4777-10T>G
- NM_001407886.1:c.4777-10T>G
- NM_001407887.1:c.4777-10T>G
- NM_001407889.1:c.4777-10T>G
- NM_001407894.1:c.4774-10T>G
- NM_001407895.1:c.4774-10T>G
- NM_001407896.1:c.4774-10T>G
- NM_001407897.1:c.4774-10T>G
- NM_001407898.1:c.4774-10T>G
- NM_001407899.1:c.4774-10T>G
- NM_001407900.1:c.4774-10T>G
- NM_001407902.1:c.4774-10T>G
- NM_001407904.1:c.4774-10T>G
- NM_001407906.1:c.4774-10T>G
- NM_001407907.1:c.4774-10T>G
- NM_001407908.1:c.4774-10T>G
- NM_001407909.1:c.4774-10T>G
- NM_001407910.1:c.4774-10T>G
- NM_001407915.1:c.4771-10T>G
- NM_001407916.1:c.4771-10T>G
- NM_001407917.1:c.4771-10T>G
- NM_001407918.1:c.4771-10T>G
- NM_001407919.1:c.4864-10T>G
- NM_001407920.1:c.4723-10T>G
- NM_001407921.1:c.4723-10T>G
- NM_001407922.1:c.4723-10T>G
- NM_001407923.1:c.4723-10T>G
- NM_001407924.1:c.4723-10T>G
- NM_001407925.1:c.4723-10T>G
- NM_001407926.1:c.4723-10T>G
- NM_001407927.1:c.4720-10T>G
- NM_001407928.1:c.4720-10T>G
- NM_001407929.1:c.4720-10T>G
- NM_001407930.1:c.4720-10T>G
- NM_001407931.1:c.4720-10T>G
- NM_001407932.1:c.4720-10T>G
- NM_001407933.1:c.4720-10T>G
- NM_001407934.1:c.4717-10T>G
- NM_001407935.1:c.4717-10T>G
- NM_001407936.1:c.4717-10T>G
- NM_001407937.1:c.4864-10T>G
- NM_001407938.1:c.4864-10T>G
- NM_001407939.1:c.4861-10T>G
- NM_001407940.1:c.4861-10T>G
- NM_001407941.1:c.4858-10T>G
- NM_001407942.1:c.4846-10T>G
- NM_001407943.1:c.4843-10T>G
- NM_001407944.1:c.4843-10T>G
- NM_001407945.1:c.4843-10T>G
- NM_001407946.1:c.4654-10T>G
- NM_001407947.1:c.4654-10T>G
- NM_001407948.1:c.4654-10T>G
- NM_001407949.1:c.4654-10T>G
- NM_001407950.1:c.4651-10T>G
- NM_001407951.1:c.4651-10T>G
- NM_001407952.1:c.4651-10T>G
- NM_001407953.1:c.4651-10T>G
- NM_001407954.1:c.4651-10T>G
- NM_001407955.1:c.4651-10T>G
- NM_001407956.1:c.4648-10T>G
- NM_001407957.1:c.4648-10T>G
- NM_001407958.1:c.4648-10T>G
- NM_001407959.1:c.4606-10T>G
- NM_001407960.1:c.4603-10T>G
- NM_001407962.1:c.4603-10T>G
- NM_001407963.1:c.4600-10T>G
- NM_001407964.1:c.4525-10T>G
- NM_001407965.1:c.4480-10T>G
- NM_001407966.1:c.4099-10T>G
- NM_001407967.1:c.4096-10T>G
- NM_001407968.1:c.2383-10T>G
- NM_001407969.1:c.2380-10T>G
- NM_001407970.1:c.1744-10T>G
- NM_001407971.1:c.1744-10T>G
- NM_001407972.1:c.1741-10T>G
- NM_001407973.1:c.1678-10T>G
- NM_001407974.1:c.1678-10T>G
- NM_001407975.1:c.1678-10T>G
- NM_001407976.1:c.1678-10T>G
- NM_001407977.1:c.1678-10T>G
- NM_001407978.1:c.1678-10T>G
- NM_001407979.1:c.1675-10T>G
- NM_001407980.1:c.1675-10T>G
- NM_001407981.1:c.1675-10T>G
- NM_001407982.1:c.1675-10T>G
- NM_001407983.1:c.1675-10T>G
- NM_001407984.1:c.1675-10T>G
- NM_001407985.1:c.1675-10T>G
- NM_001407986.1:c.1675-10T>G
- NM_001407990.1:c.1675-10T>G
- NM_001407991.1:c.1675-10T>G
- NM_001407992.1:c.1675-10T>G
- NM_001407993.1:c.1675-10T>G
- NM_001408392.1:c.1672-10T>G
- NM_001408396.1:c.1672-10T>G
- NM_001408397.1:c.1672-10T>G
- NM_001408398.1:c.1672-10T>G
- NM_001408399.1:c.1672-10T>G
- NM_001408400.1:c.1672-10T>G
- NM_001408401.1:c.1672-10T>G
- NM_001408402.1:c.1672-10T>G
- NM_001408403.1:c.1672-10T>G
- NM_001408404.1:c.1672-10T>G
- NM_001408406.1:c.1669-10T>G
- NM_001408407.1:c.1669-10T>G
- NM_001408408.1:c.1669-10T>G
- NM_001408409.1:c.1666-10T>G
- NM_001408410.1:c.1603-10T>G
- NM_001408411.1:c.1600-10T>G
- NM_001408412.1:c.1597-10T>G
- NM_001408413.1:c.1597-10T>G
- NM_001408414.1:c.1597-10T>G
- NM_001408415.1:c.1597-10T>G
- NM_001408416.1:c.1597-10T>G
- NM_001408418.1:c.1561-10T>G
- NM_001408419.1:c.1561-10T>G
- NM_001408420.1:c.1561-10T>G
- NM_001408421.1:c.1558-10T>G
- NM_001408422.1:c.1558-10T>G
- NM_001408423.1:c.1558-10T>G
- NM_001408424.1:c.1558-10T>G
- NM_001408425.1:c.1555-10T>G
- NM_001408426.1:c.1555-10T>G
- NM_001408427.1:c.1555-10T>G
- NM_001408428.1:c.1555-10T>G
- NM_001408429.1:c.1555-10T>G
- NM_001408430.1:c.1555-10T>G
- NM_001408431.1:c.1555-10T>G
- NM_001408432.1:c.1552-10T>G
- NM_001408433.1:c.1552-10T>G
- NM_001408434.1:c.1552-10T>G
- NM_001408435.1:c.1552-10T>G
- NM_001408436.1:c.1552-10T>G
- NM_001408437.1:c.1552-10T>G
- NM_001408438.1:c.1552-10T>G
- NM_001408439.1:c.1552-10T>G
- NM_001408440.1:c.1552-10T>G
- NM_001408441.1:c.1552-10T>G
- NM_001408442.1:c.1552-10T>G
- NM_001408443.1:c.1552-10T>G
- NM_001408444.1:c.1552-10T>G
- NM_001408445.1:c.1549-10T>G
- NM_001408446.1:c.1549-10T>G
- NM_001408447.1:c.1549-10T>G
- NM_001408448.1:c.1549-10T>G
- NM_001408450.1:c.1549-10T>G
- NM_001408451.1:c.1543-10T>G
- NM_001408452.1:c.1537-10T>G
- NM_001408453.1:c.1537-10T>G
- NM_001408454.1:c.1537-10T>G
- NM_001408455.1:c.1537-10T>G
- NM_001408456.1:c.1537-10T>G
- NM_001408457.1:c.1537-10T>G
- NM_001408458.1:c.1534-10T>G
- NM_001408459.1:c.1534-10T>G
- NM_001408460.1:c.1534-10T>G
- NM_001408461.1:c.1534-10T>G
- NM_001408462.1:c.1534-10T>G
- NM_001408463.1:c.1534-10T>G
- NM_001408464.1:c.1534-10T>G
- NM_001408465.1:c.1534-10T>G
- NM_001408466.1:c.1534-10T>G
- NM_001408467.1:c.1534-10T>G
- NM_001408468.1:c.1531-10T>G
- NM_001408469.1:c.1531-10T>G
- NM_001408470.1:c.1531-10T>G
- NM_001408472.1:c.1675-10T>G
- NM_001408473.1:c.1672-10T>G
- NM_001408474.1:c.1477-10T>G
- NM_001408475.1:c.1474-10T>G
- NM_001408476.1:c.1474-10T>G
- NM_001408478.1:c.1468-10T>G
- NM_001408479.1:c.1468-10T>G
- NM_001408480.1:c.1468-10T>G
- NM_001408481.1:c.1465-10T>G
- NM_001408482.1:c.1465-10T>G
- NM_001408483.1:c.1465-10T>G
- NM_001408484.1:c.1465-10T>G
- NM_001408485.1:c.1465-10T>G
- NM_001408489.1:c.1465-10T>G
- NM_001408490.1:c.1465-10T>G
- NM_001408491.1:c.1465-10T>G
- NM_001408492.1:c.1462-10T>G
- NM_001408493.1:c.1462-10T>G
- NM_001408494.1:c.1438-10T>G
- NM_001408495.1:c.1432-10T>G
- NM_001408496.1:c.1414-10T>G
- NM_001408497.1:c.1414-10T>G
- NM_001408498.1:c.1414-10T>G
- NM_001408499.1:c.1414-10T>G
- NM_001408500.1:c.1414-10T>G
- NM_001408501.1:c.1414-10T>G
- NM_001408502.1:c.1411-10T>G
- NM_001408503.1:c.1411-10T>G
- NM_001408504.1:c.1411-10T>G
- NM_001408505.1:c.1408-10T>G
- NM_001408506.1:c.1351-10T>G
- NM_001408507.1:c.1348-10T>G
- NM_001408508.1:c.1339-10T>G
- NM_001408509.1:c.1336-10T>G
- NM_001408510.1:c.1297-10T>G
- NM_001408511.1:c.1294-10T>G
- NM_001408512.1:c.1174-10T>G
- NM_001408513.1:c.1147-10T>G
- NM_001408514.1:c.839-3754T>G
- NM_007294.4:c.4987-10T>GMANE SELECT
- NM_007297.4:c.4846-10T>G
- NM_007298.4:c.1675-10T>G
- NM_007299.4:c.1675-10T>G
- NM_007300.4:c.5050-10T>G
- LRG_292t1:c.4987-10T>G
- LRG_292:g.150279T>G
- NC_000017.10:g.41219722A>C
- NM_007294.3:c.4987-10T>G
This HGVS expression did not pass validation- Links:
- dbSNP: rs1555579828
- NCBI 1000 Genomes Browser:
- rs1555579828
- Molecular consequence:
- NM_001407571.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407581.1:c.5053-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407582.1:c.5053-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407583.1:c.5050-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407585.1:c.5050-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407587.1:c.5050-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407590.1:c.5047-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407591.1:c.5047-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407593.1:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407594.1:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407596.1:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407597.1:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407598.1:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407602.1:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407603.1:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407605.1:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407610.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407611.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407612.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407613.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407614.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407615.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407616.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407617.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407618.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407619.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407620.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407621.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407622.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407623.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407624.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407625.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407626.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407627.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407628.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407629.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407630.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407631.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407632.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407633.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407634.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407635.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407636.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407637.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407638.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407639.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407640.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407641.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407642.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407644.1:c.4978-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407645.1:c.4978-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407646.1:c.4975-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407647.1:c.4972-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407648.1:c.4930-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407649.1:c.4927-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407652.1:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407653.1:c.4909-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407654.1:c.4909-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407655.1:c.4909-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407656.1:c.4906-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407657.1:c.4906-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407658.1:c.4906-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407659.1:c.4903-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407660.1:c.4903-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407661.1:c.4903-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407662.1:c.4903-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407663.1:c.4903-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407664.1:c.4864-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407665.1:c.4864-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407666.1:c.4864-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407667.1:c.4864-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407668.1:c.4864-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407669.1:c.4864-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407670.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407671.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407672.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407673.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407674.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407675.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407676.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407677.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407678.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407679.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407680.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407681.1:c.4858-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407682.1:c.4858-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407683.1:c.4858-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407684.1:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407685.1:c.4858-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407686.1:c.4858-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407687.1:c.4858-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407688.1:c.4858-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407689.1:c.4858-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407690.1:c.4855-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407691.1:c.4855-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407692.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407694.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407695.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407696.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407697.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407698.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407724.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407725.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407726.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407727.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407728.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407729.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407730.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407731.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407732.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407733.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407734.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407735.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407736.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407737.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407738.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407739.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407740.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407741.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407742.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407743.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407744.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407745.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407746.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407747.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407748.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407749.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407750.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407751.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407752.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407838.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407839.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407841.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407842.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407843.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407844.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407845.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407846.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407847.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407848.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407849.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407850.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407851.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407852.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407853.1:c.4840-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407854.1:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407858.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407859.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407860.1:c.4984-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407861.1:c.4981-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407862.1:c.4786-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407863.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407874.1:c.4780-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407875.1:c.4780-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407879.1:c.4777-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407881.1:c.4777-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407882.1:c.4777-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407884.1:c.4777-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407885.1:c.4777-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407886.1:c.4777-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407887.1:c.4777-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407889.1:c.4777-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407894.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407895.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407896.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407897.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407898.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407899.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407900.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407902.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407904.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407906.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407907.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407908.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407909.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407910.1:c.4774-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407915.1:c.4771-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407916.1:c.4771-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407917.1:c.4771-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407918.1:c.4771-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407919.1:c.4864-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407920.1:c.4723-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407921.1:c.4723-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407922.1:c.4723-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407923.1:c.4723-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407924.1:c.4723-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407925.1:c.4723-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407926.1:c.4723-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407927.1:c.4720-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407928.1:c.4720-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407929.1:c.4720-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407930.1:c.4720-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407931.1:c.4720-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407932.1:c.4720-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407933.1:c.4720-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407934.1:c.4717-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407935.1:c.4717-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407936.1:c.4717-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407937.1:c.4864-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407938.1:c.4864-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407939.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407940.1:c.4861-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407941.1:c.4858-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407942.1:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407943.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407944.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407945.1:c.4843-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407946.1:c.4654-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407947.1:c.4654-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407948.1:c.4654-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407949.1:c.4654-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407950.1:c.4651-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407951.1:c.4651-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407952.1:c.4651-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407953.1:c.4651-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407954.1:c.4651-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407955.1:c.4651-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407956.1:c.4648-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407957.1:c.4648-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407958.1:c.4648-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407959.1:c.4606-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407960.1:c.4603-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407962.1:c.4603-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407963.1:c.4600-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407964.1:c.4525-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407965.1:c.4480-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407966.1:c.4099-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407967.1:c.4096-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407968.1:c.2383-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407969.1:c.2380-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407970.1:c.1744-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407971.1:c.1744-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407972.1:c.1741-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407973.1:c.1678-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407974.1:c.1678-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407975.1:c.1678-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407976.1:c.1678-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407977.1:c.1678-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407978.1:c.1678-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407979.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407980.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407981.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407982.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407983.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407984.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407985.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407986.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407990.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407991.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407992.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407993.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408392.1:c.1672-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408396.1:c.1672-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408397.1:c.1672-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408398.1:c.1672-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408399.1:c.1672-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408400.1:c.1672-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408401.1:c.1672-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408402.1:c.1672-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408403.1:c.1672-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408404.1:c.1672-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408406.1:c.1669-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408407.1:c.1669-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408408.1:c.1669-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408409.1:c.1666-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408410.1:c.1603-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408411.1:c.1600-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408412.1:c.1597-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408413.1:c.1597-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408414.1:c.1597-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408415.1:c.1597-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408416.1:c.1597-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408418.1:c.1561-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408419.1:c.1561-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408420.1:c.1561-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408421.1:c.1558-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408422.1:c.1558-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408423.1:c.1558-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408424.1:c.1558-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408425.1:c.1555-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408426.1:c.1555-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408427.1:c.1555-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408428.1:c.1555-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408429.1:c.1555-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408430.1:c.1555-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408431.1:c.1555-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408432.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408433.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408434.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408435.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408436.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408437.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408438.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408439.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408440.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408441.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408442.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408443.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408444.1:c.1552-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408445.1:c.1549-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408446.1:c.1549-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408447.1:c.1549-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408448.1:c.1549-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408450.1:c.1549-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408451.1:c.1543-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408452.1:c.1537-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408453.1:c.1537-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408454.1:c.1537-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408455.1:c.1537-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408456.1:c.1537-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408457.1:c.1537-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408458.1:c.1534-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408459.1:c.1534-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408460.1:c.1534-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408461.1:c.1534-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408462.1:c.1534-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408463.1:c.1534-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408464.1:c.1534-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408465.1:c.1534-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408466.1:c.1534-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408467.1:c.1534-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408468.1:c.1531-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408469.1:c.1531-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408470.1:c.1531-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408472.1:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408473.1:c.1672-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408474.1:c.1477-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408475.1:c.1474-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408476.1:c.1474-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408478.1:c.1468-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408479.1:c.1468-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408480.1:c.1468-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408481.1:c.1465-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408482.1:c.1465-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408483.1:c.1465-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408484.1:c.1465-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408485.1:c.1465-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408489.1:c.1465-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408490.1:c.1465-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408491.1:c.1465-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408492.1:c.1462-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408493.1:c.1462-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408494.1:c.1438-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408495.1:c.1432-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408496.1:c.1414-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408497.1:c.1414-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408498.1:c.1414-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408499.1:c.1414-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408500.1:c.1414-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408501.1:c.1414-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408502.1:c.1411-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408503.1:c.1411-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408504.1:c.1411-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408505.1:c.1408-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408506.1:c.1351-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408507.1:c.1348-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408508.1:c.1339-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408509.1:c.1336-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408510.1:c.1297-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408511.1:c.1294-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408512.1:c.1174-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408513.1:c.1147-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408514.1:c.839-3754T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_007294.4:c.4987-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_007297.4:c.4846-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_007298.4:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_007299.4:c.1675-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_007300.4:c.5050-10T>G - intron variant - [Sequence Ontology: SO:0001627]
- Functional consequence:
- function_uncertain_variant [Sequence Ontology: SO:0002220] - Comment(s)
- The saturation genome editing (SGE) assay for BRCA1 NM_007294.3:c.4987-10T>G, a INTRONIC variant, produced a function score of -0.95, corresponding to a functional classification of INTERMEDIATE. SGE function score ranges for classification are as follows: ‘functional’, score > -0.748; ‘intermediate’, -0.748 > score > -1.328; ‘non-functional’, score < -1.328. The median synonymous SNV scored 0.0 and the median nonsense SNV scored -2.12.
Condition(s)
- Name:
- Hereditary breast ovarian cancer syndrome
- Synonyms:
- Hereditary breast and ovarian cancer syndrome; Hereditary breast and ovarian cancer; Hereditary breast and ovarian cancer syndrome (HBOC); See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0003582; MeSH: D061325; MedGen: C0677776; Orphanet: 145
-
PREDICTED: uncharacterized protein LOC103492217 isoform X2 [Cucumis melo]
PREDICTED: uncharacterized protein LOC103492217 isoform X2 [Cucumis melo]gi|659099677|ref|XP_008450722.1|Protein
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See more...Assertion and evidence details
Submission Accession | Submitter | Review Status (Assertion method) | Clinical Significance (Last evaluated) | Origin | Method | Citations |
---|---|---|---|---|---|---|
SCV004445265 | Labcorp Genetics (formerly Invitae), Labcorp | criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) | Uncertain significance (Mar 15, 2023) | germline | clinical testing |
Summary from all submissions
Ethnicity | Origin | Affected | Individuals | Families | Chromosomes tested | Number Tested | Family history | Method |
---|---|---|---|---|---|---|---|---|
not provided | germline | unknown | not provided | not provided | not provided | not provided | not provided | clinical 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.
- PMID:
- 30209399
- PMCID:
- PMC6181777
Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.
Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.
Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.
- PMID:
- 28492532
- PMCID:
- PMC5632818
Details of each submission
From Labcorp Genetics (formerly Invitae), Labcorp, SCV004445265.1
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | PubMed (2) |
Description
In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. Experimental studies are conflicting or provide insufficient evidence to determine the effect of this variant on BRCA1 function (PMID: 30209399). ClinVar contains an entry for this variant (Variation ID: 496387). This variant has not been reported in the literature in individuals affected with BRCA1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change falls in intron 15 of the BRCA1 gene. It does not directly change the encoded amino acid sequence of the BRCA1 protein.
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | unknown | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
Last Updated: Oct 8, 2024