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NM_007294.4(BRCA1):c.670+8C>T AND Breast-ovarian cancer, familial, susceptibility to, 1

Germline classification:
Conflicting interpretations of pathogenicity (2 submissions)
Last evaluated:
Jun 24, 2009
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria 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:
RCV000031273.9

Allele description [Variation Report for NM_007294.4(BRCA1):c.670+8C>T]

NM_007294.4(BRCA1):c.670+8C>T

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.670+8C>T
HGVS:
  • NC_000017.11:g.43095838G>A
  • NG_005905.2:g.122146C>T
  • NM_001407571.1:c.457+8C>T
  • NM_001407581.1:c.670+8C>T
  • NM_001407582.1:c.670+8C>T
  • NM_001407583.1:c.670+8C>T
  • NM_001407585.1:c.670+8C>T
  • NM_001407587.1:c.667+8C>T
  • NM_001407590.1:c.667+8C>T
  • NM_001407591.1:c.667+8C>T
  • NM_001407593.1:c.670+8C>T
  • NM_001407594.1:c.670+8C>T
  • NM_001407596.1:c.670+8C>T
  • NM_001407597.1:c.670+8C>T
  • NM_001407598.1:c.670+8C>T
  • NM_001407602.1:c.670+8C>T
  • NM_001407603.1:c.670+8C>T
  • NM_001407605.1:c.670+8C>T
  • NM_001407610.1:c.667+8C>T
  • NM_001407611.1:c.667+8C>T
  • NM_001407612.1:c.667+8C>T
  • NM_001407613.1:c.667+8C>T
  • NM_001407614.1:c.667+8C>T
  • NM_001407615.1:c.667+8C>T
  • NM_001407616.1:c.670+8C>T
  • NM_001407617.1:c.670+8C>T
  • NM_001407618.1:c.670+8C>T
  • NM_001407619.1:c.670+8C>T
  • NM_001407620.1:c.670+8C>T
  • NM_001407621.1:c.670+8C>T
  • NM_001407622.1:c.670+8C>T
  • NM_001407623.1:c.670+8C>T
  • NM_001407624.1:c.670+8C>T
  • NM_001407625.1:c.670+8C>T
  • NM_001407626.1:c.670+8C>T
  • NM_001407627.1:c.667+8C>T
  • NM_001407628.1:c.667+8C>T
  • NM_001407629.1:c.667+8C>T
  • NM_001407630.1:c.667+8C>T
  • NM_001407631.1:c.667+8C>T
  • NM_001407632.1:c.667+8C>T
  • NM_001407633.1:c.667+8C>T
  • NM_001407634.1:c.667+8C>T
  • NM_001407635.1:c.667+8C>T
  • NM_001407636.1:c.667+8C>T
  • NM_001407637.1:c.667+8C>T
  • NM_001407638.1:c.667+8C>T
  • NM_001407639.1:c.670+8C>T
  • NM_001407640.1:c.670+8C>T
  • NM_001407641.1:c.670+8C>T
  • NM_001407642.1:c.670+8C>T
  • NM_001407644.1:c.667+8C>T
  • NM_001407645.1:c.667+8C>T
  • NM_001407646.1:c.661+8C>T
  • NM_001407647.1:c.661+8C>T
  • NM_001407648.1:c.548-978C>T
  • NM_001407649.1:c.545-978C>T
  • NM_001407652.1:c.670+8C>T
  • NM_001407653.1:c.592+8C>T
  • NM_001407654.1:c.592+8C>T
  • NM_001407655.1:c.592+8C>T
  • NM_001407656.1:c.592+8C>T
  • NM_001407657.1:c.592+8C>T
  • NM_001407658.1:c.592+8C>T
  • NM_001407659.1:c.589+8C>T
  • NM_001407660.1:c.589+8C>T
  • NM_001407661.1:c.589+8C>T
  • NM_001407662.1:c.589+8C>T
  • NM_001407663.1:c.592+8C>T
  • NM_001407664.1:c.548-978C>T
  • NM_001407665.1:c.548-978C>T
  • NM_001407666.1:c.548-978C>T
  • NM_001407667.1:c.548-978C>T
  • NM_001407668.1:c.548-978C>T
  • NM_001407669.1:c.548-978C>T
  • NM_001407670.1:c.545-978C>T
  • NM_001407671.1:c.545-978C>T
  • NM_001407672.1:c.545-978C>T
  • NM_001407673.1:c.545-978C>T
  • NM_001407674.1:c.548-978C>T
  • NM_001407675.1:c.548-978C>T
  • NM_001407676.1:c.548-978C>T
  • NM_001407677.1:c.548-978C>T
  • NM_001407678.1:c.548-978C>T
  • NM_001407679.1:c.548-978C>T
  • NM_001407680.1:c.548-978C>T
  • NM_001407681.1:c.548-978C>T
  • NM_001407682.1:c.548-978C>T
  • NM_001407683.1:c.548-978C>T
  • NM_001407684.1:c.670+8C>T
  • NM_001407685.1:c.545-978C>T
  • NM_001407686.1:c.545-978C>T
  • NM_001407687.1:c.545-978C>T
  • NM_001407688.1:c.545-978C>T
  • NM_001407689.1:c.545-978C>T
  • NM_001407690.1:c.545-978C>T
  • NM_001407691.1:c.545-978C>T
  • NM_001407692.1:c.529+8C>T
  • NM_001407694.1:c.529+8C>T
  • NM_001407695.1:c.529+8C>T
  • NM_001407696.1:c.529+8C>T
  • NM_001407697.1:c.529+8C>T
  • NM_001407698.1:c.529+8C>T
  • NM_001407724.1:c.529+8C>T
  • NM_001407725.1:c.529+8C>T
  • NM_001407726.1:c.529+8C>T
  • NM_001407727.1:c.529+8C>T
  • NM_001407728.1:c.529+8C>T
  • NM_001407729.1:c.529+8C>T
  • NM_001407730.1:c.529+8C>T
  • NM_001407731.1:c.529+8C>T
  • NM_001407732.1:c.529+8C>T
  • NM_001407733.1:c.529+8C>T
  • NM_001407734.1:c.529+8C>T
  • NM_001407735.1:c.529+8C>T
  • NM_001407736.1:c.529+8C>T
  • NM_001407737.1:c.529+8C>T
  • NM_001407738.1:c.529+8C>T
  • NM_001407739.1:c.529+8C>T
  • NM_001407740.1:c.526+8C>T
  • NM_001407741.1:c.526+8C>T
  • NM_001407742.1:c.526+8C>T
  • NM_001407743.1:c.526+8C>T
  • NM_001407744.1:c.526+8C>T
  • NM_001407745.1:c.526+8C>T
  • NM_001407746.1:c.526+8C>T
  • NM_001407747.1:c.526+8C>T
  • NM_001407748.1:c.526+8C>T
  • NM_001407749.1:c.526+8C>T
  • NM_001407750.1:c.529+8C>T
  • NM_001407751.1:c.529+8C>T
  • NM_001407752.1:c.529+8C>T
  • NM_001407838.1:c.526+8C>T
  • NM_001407839.1:c.526+8C>T
  • NM_001407841.1:c.526+8C>T
  • NM_001407842.1:c.526+8C>T
  • NM_001407843.1:c.526+8C>T
  • NM_001407844.1:c.526+8C>T
  • NM_001407845.1:c.526+8C>T
  • NM_001407846.1:c.526+8C>T
  • NM_001407847.1:c.526+8C>T
  • NM_001407848.1:c.526+8C>T
  • NM_001407849.1:c.526+8C>T
  • NM_001407850.1:c.529+8C>T
  • NM_001407851.1:c.529+8C>T
  • NM_001407852.1:c.529+8C>T
  • NM_001407853.1:c.457+8C>T
  • NM_001407854.1:c.670+8C>T
  • NM_001407858.1:c.670+8C>T
  • NM_001407859.1:c.670+8C>T
  • NM_001407860.1:c.667+8C>T
  • NM_001407861.1:c.667+8C>T
  • NM_001407862.1:c.470-978C>T
  • NM_001407863.1:c.548-978C>T
  • NM_001407874.1:c.467-978C>T
  • NM_001407875.1:c.467-978C>T
  • NM_001407879.1:c.460+8C>T
  • NM_001407881.1:c.460+8C>T
  • NM_001407882.1:c.460+8C>T
  • NM_001407884.1:c.460+8C>T
  • NM_001407885.1:c.460+8C>T
  • NM_001407886.1:c.460+8C>T
  • NM_001407887.1:c.460+8C>T
  • NM_001407889.1:c.460+8C>T
  • NM_001407894.1:c.457+8C>T
  • NM_001407895.1:c.457+8C>T
  • NM_001407896.1:c.457+8C>T
  • NM_001407897.1:c.457+8C>T
  • NM_001407898.1:c.457+8C>T
  • NM_001407899.1:c.457+8C>T
  • NM_001407900.1:c.460+8C>T
  • NM_001407902.1:c.460+8C>T
  • NM_001407904.1:c.460+8C>T
  • NM_001407906.1:c.460+8C>T
  • NM_001407907.1:c.460+8C>T
  • NM_001407908.1:c.460+8C>T
  • NM_001407909.1:c.460+8C>T
  • NM_001407910.1:c.460+8C>T
  • NM_001407915.1:c.457+8C>T
  • NM_001407916.1:c.457+8C>T
  • NM_001407917.1:c.457+8C>T
  • NM_001407918.1:c.457+8C>T
  • NM_001407919.1:c.548-978C>T
  • NM_001407920.1:c.407-978C>T
  • NM_001407921.1:c.407-978C>T
  • NM_001407922.1:c.407-978C>T
  • NM_001407923.1:c.407-978C>T
  • NM_001407924.1:c.407-978C>T
  • NM_001407925.1:c.407-978C>T
  • NM_001407926.1:c.407-978C>T
  • NM_001407927.1:c.407-978C>T
  • NM_001407928.1:c.407-978C>T
  • NM_001407929.1:c.407-978C>T
  • NM_001407930.1:c.404-978C>T
  • NM_001407931.1:c.404-978C>T
  • NM_001407932.1:c.404-978C>T
  • NM_001407933.1:c.407-978C>T
  • NM_001407934.1:c.404-978C>T
  • NM_001407935.1:c.407-978C>T
  • NM_001407936.1:c.404-978C>T
  • NM_001407937.1:c.548-978C>T
  • NM_001407938.1:c.548-978C>T
  • NM_001407939.1:c.548-978C>T
  • NM_001407940.1:c.545-978C>T
  • NM_001407941.1:c.545-978C>T
  • NM_001407942.1:c.529+8C>T
  • NM_001407943.1:c.526+8C>T
  • NM_001407944.1:c.529+8C>T
  • NM_001407945.1:c.529+8C>T
  • NM_001407946.1:c.338-978C>T
  • NM_001407947.1:c.338-978C>T
  • NM_001407948.1:c.338-978C>T
  • NM_001407949.1:c.338-978C>T
  • NM_001407950.1:c.338-978C>T
  • NM_001407951.1:c.338-978C>T
  • NM_001407952.1:c.338-978C>T
  • NM_001407953.1:c.338-978C>T
  • NM_001407954.1:c.335-978C>T
  • NM_001407955.1:c.335-978C>T
  • NM_001407956.1:c.335-978C>T
  • NM_001407957.1:c.338-978C>T
  • NM_001407958.1:c.335-978C>T
  • NM_001407959.1:c.289+8C>T
  • NM_001407960.1:c.289+8C>T
  • NM_001407962.1:c.286+8C>T
  • NM_001407963.1:c.289+8C>T
  • NM_001407964.1:c.526+8C>T
  • NM_001407965.1:c.167-978C>T
  • NM_001407966.1:c.-218-978C>T
  • NM_001407967.1:c.-218-978C>T
  • NM_001407968.1:c.670+8C>T
  • NM_001407969.1:c.670+8C>T
  • NM_001407970.1:c.670+8C>T
  • NM_001407971.1:c.670+8C>T
  • NM_001407972.1:c.667+8C>T
  • NM_001407973.1:c.670+8C>T
  • NM_001407974.1:c.670+8C>T
  • NM_001407975.1:c.670+8C>T
  • NM_001407976.1:c.670+8C>T
  • NM_001407977.1:c.670+8C>T
  • NM_001407978.1:c.670+8C>T
  • NM_001407979.1:c.670+8C>T
  • NM_001407980.1:c.670+8C>T
  • NM_001407981.1:c.670+8C>T
  • NM_001407982.1:c.670+8C>T
  • NM_001407983.1:c.670+8C>T
  • NM_001407984.1:c.667+8C>T
  • NM_001407985.1:c.667+8C>T
  • NM_001407986.1:c.667+8C>T
  • NM_001407990.1:c.670+8C>T
  • NM_001407991.1:c.667+8C>T
  • NM_001407992.1:c.667+8C>T
  • NM_001407993.1:c.670+8C>T
  • NM_001408392.1:c.667+8C>T
  • NM_001408396.1:c.667+8C>T
  • NM_001408397.1:c.667+8C>T
  • NM_001408398.1:c.667+8C>T
  • NM_001408399.1:c.667+8C>T
  • NM_001408400.1:c.667+8C>T
  • NM_001408401.1:c.667+8C>T
  • NM_001408402.1:c.667+8C>T
  • NM_001408403.1:c.670+8C>T
  • NM_001408404.1:c.670+8C>T
  • NM_001408406.1:c.670+8C>T
  • NM_001408407.1:c.667+8C>T
  • NM_001408408.1:c.661+8C>T
  • NM_001408409.1:c.592+8C>T
  • NM_001408410.1:c.529+8C>T
  • NM_001408411.1:c.592+8C>T
  • NM_001408412.1:c.592+8C>T
  • NM_001408413.1:c.589+8C>T
  • NM_001408414.1:c.592+8C>T
  • NM_001408415.1:c.592+8C>T
  • NM_001408416.1:c.589+8C>T
  • NM_001408418.1:c.670+8C>T
  • NM_001408419.1:c.670+8C>T
  • NM_001408420.1:c.670+8C>T
  • NM_001408421.1:c.667+8C>T
  • NM_001408422.1:c.670+8C>T
  • NM_001408423.1:c.670+8C>T
  • NM_001408424.1:c.667+8C>T
  • NM_001408425.1:c.548-978C>T
  • NM_001408426.1:c.548-978C>T
  • NM_001408427.1:c.548-978C>T
  • NM_001408428.1:c.548-978C>T
  • NM_001408429.1:c.548-978C>T
  • NM_001408430.1:c.548-978C>T
  • NM_001408431.1:c.667+8C>T
  • NM_001408432.1:c.545-978C>T
  • NM_001408433.1:c.545-978C>T
  • NM_001408434.1:c.545-978C>T
  • NM_001408435.1:c.545-978C>T
  • NM_001408436.1:c.548-978C>T
  • NM_001408437.1:c.548-978C>T
  • NM_001408438.1:c.548-978C>T
  • NM_001408439.1:c.548-978C>T
  • NM_001408440.1:c.548-978C>T
  • NM_001408441.1:c.548-978C>T
  • NM_001408442.1:c.548-978C>T
  • NM_001408443.1:c.548-978C>T
  • NM_001408444.1:c.548-978C>T
  • NM_001408445.1:c.545-978C>T
  • NM_001408446.1:c.545-978C>T
  • NM_001408447.1:c.545-978C>T
  • NM_001408448.1:c.545-978C>T
  • NM_001408450.1:c.545-978C>T
  • NM_001408451.1:c.535+8C>T
  • NM_001408452.1:c.529+8C>T
  • NM_001408453.1:c.529+8C>T
  • NM_001408454.1:c.529+8C>T
  • NM_001408455.1:c.529+8C>T
  • NM_001408456.1:c.529+8C>T
  • NM_001408457.1:c.529+8C>T
  • NM_001408458.1:c.529+8C>T
  • NM_001408459.1:c.529+8C>T
  • NM_001408460.1:c.529+8C>T
  • NM_001408461.1:c.529+8C>T
  • NM_001408462.1:c.526+8C>T
  • NM_001408463.1:c.526+8C>T
  • NM_001408464.1:c.526+8C>T
  • NM_001408465.1:c.526+8C>T
  • NM_001408466.1:c.529+8C>T
  • NM_001408467.1:c.529+8C>T
  • NM_001408468.1:c.526+8C>T
  • NM_001408469.1:c.529+8C>T
  • NM_001408470.1:c.526+8C>T
  • NM_001408472.1:c.670+8C>T
  • NM_001408473.1:c.667+8C>T
  • NM_001408474.1:c.470-978C>T
  • NM_001408475.1:c.467-978C>T
  • NM_001408476.1:c.470-978C>T
  • NM_001408478.1:c.460+8C>T
  • NM_001408479.1:c.460+8C>T
  • NM_001408480.1:c.460+8C>T
  • NM_001408481.1:c.460+8C>T
  • NM_001408482.1:c.460+8C>T
  • NM_001408483.1:c.460+8C>T
  • NM_001408484.1:c.460+8C>T
  • NM_001408485.1:c.460+8C>T
  • NM_001408489.1:c.460+8C>T
  • NM_001408490.1:c.457+8C>T
  • NM_001408491.1:c.457+8C>T
  • NM_001408492.1:c.460+8C>T
  • NM_001408493.1:c.457+8C>T
  • NM_001408494.1:c.547+3937C>T
  • NM_001408495.1:c.544+3937C>T
  • NM_001408496.1:c.407-978C>T
  • NM_001408497.1:c.407-978C>T
  • NM_001408498.1:c.407-978C>T
  • NM_001408499.1:c.407-978C>T
  • NM_001408500.1:c.407-978C>T
  • NM_001408501.1:c.407-978C>T
  • NM_001408502.1:c.338-978C>T
  • NM_001408503.1:c.404-978C>T
  • NM_001408504.1:c.404-978C>T
  • NM_001408505.1:c.404-978C>T
  • NM_001408506.1:c.460+8C>T
  • NM_001408507.1:c.460+8C>T
  • NM_001408508.1:c.335-978C>T
  • NM_001408509.1:c.335-978C>T
  • NM_001408510.1:c.289+8C>T
  • NM_001408511.1:c.403+3937C>T
  • NM_001408512.1:c.167-978C>T
  • NM_001408513.1:c.460+8C>T
  • NM_001408514.1:c.460+8C>T
  • NM_007294.4:c.670+8C>TMANE SELECT
  • NM_007297.4:c.529+8C>T
  • NM_007298.4:c.670+8C>T
  • NM_007299.4:c.670+8C>T
  • NM_007300.4:c.670+8C>T
  • LRG_292t1:c.670+8C>T
  • LRG_292:g.122146C>T
  • NC_000017.10:g.41247855G>A
  • NM_007294.3:c.670+8C>T
  • NM_007300.3:c.670+8C>T
  • U14680.1:n.789+8C>T
Nucleotide change:
IVS10+8C>T
Links:
Breast Cancer Information Core (BIC) (BRCA1): 789+8&base_change=C to T; dbSNP: rs80358050
NCBI 1000 Genomes Browser:
rs80358050
Molecular consequence:
  • NM_001407571.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407581.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407582.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407583.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407585.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407587.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407590.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407591.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407593.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407594.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407596.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407597.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407598.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407602.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407603.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407605.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407610.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407611.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407612.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407613.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407614.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407615.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407616.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407617.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407618.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407619.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407620.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407621.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407622.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407623.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407624.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407625.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407626.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407627.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407628.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407629.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407630.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407631.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407632.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407633.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407634.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407635.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407636.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407637.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407638.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407639.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407640.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407641.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407642.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407644.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407645.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407646.1:c.661+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407647.1:c.661+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407648.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407649.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407652.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407653.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407654.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407655.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407656.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407657.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407658.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407659.1:c.589+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407660.1:c.589+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407661.1:c.589+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407662.1:c.589+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407663.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407664.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407665.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407666.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407667.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407668.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407669.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407670.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407671.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407672.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407673.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407674.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407675.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407676.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407677.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407678.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407679.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407680.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407681.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407682.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407683.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407684.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407685.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407686.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407687.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407688.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407689.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407690.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407691.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407692.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407694.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407695.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407696.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407697.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407698.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407724.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407725.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407726.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407727.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407728.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407729.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407730.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407731.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407732.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407733.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407734.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407735.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407736.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407737.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407738.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407739.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407740.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407741.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407742.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407743.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407744.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407745.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407746.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407747.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407748.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407749.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407750.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407751.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407752.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407838.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407839.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407841.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407842.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407843.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407844.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407845.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407846.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407847.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407848.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407849.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407850.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407851.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407852.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407853.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407854.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407858.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407859.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407860.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407861.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407862.1:c.470-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407863.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407874.1:c.467-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407875.1:c.467-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407879.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407881.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407882.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407884.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407885.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407886.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407887.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407889.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407894.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407895.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407896.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407897.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407898.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407899.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407900.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407902.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407904.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407906.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407907.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407908.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407909.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407910.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407915.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407916.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407917.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407918.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407919.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407920.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407921.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407922.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407923.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407924.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407925.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407926.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407927.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407928.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407929.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407930.1:c.404-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407931.1:c.404-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407932.1:c.404-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407933.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407934.1:c.404-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407935.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407936.1:c.404-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407937.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407938.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407939.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407940.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407941.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407942.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407943.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407944.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407945.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407946.1:c.338-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407947.1:c.338-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407948.1:c.338-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407949.1:c.338-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407950.1:c.338-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407951.1:c.338-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407952.1:c.338-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407953.1:c.338-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407954.1:c.335-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407955.1:c.335-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407956.1:c.335-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407957.1:c.338-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407958.1:c.335-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407959.1:c.289+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407960.1:c.289+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407962.1:c.286+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407963.1:c.289+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407964.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407965.1:c.167-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407966.1:c.-218-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407967.1:c.-218-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407968.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407969.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407970.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.661+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.589+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.592+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.589+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.548-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.545-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.535+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.526+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.667+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.470-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.467-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.470-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.457+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.547+3937C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.544+3937C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.407-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.338-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.404-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.404-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.404-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.335-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.335-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.289+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.403+3937C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.167-978C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.460+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007294.4:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007297.4:c.529+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007300.4:c.670+8C>T - intron variant - [Sequence Ontology: SO:0001627]
Observations:
3

Condition(s)

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

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000053878Sharing Clinical Reports Project (SCRP)
no assertion criteria provided
Likely benign
(Jun 24, 2009) 		germlineclinical testing

SCV000145653Breast Cancer Information Core (BIC) (BRCA1)
no assertion criteria provided
Uncertain significance
(Feb 20, 2004) 		germlineclinical testing

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot provided2not providednot provided2not providedclinical testing
Western Europeangermlineyes1not providednot providednot providednot providedclinical testing

Details of each submission

From Sharing Clinical Reports Project (SCRP), SCV000053878.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot provided2not providednot providednot providednot providednot providednot provided

From Breast Cancer Information Core (BIC) (BRCA1), SCV000145653.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1Western European1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

Last Updated: Jul 15, 2024