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NM_007294.4(BRCA1):c.5407-16C>T AND Breast-ovarian cancer, familial, susceptibility to, 1

Germline classification:
Likely benign (1 submission)
Last evaluated:
Feb 25, 2011
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:
RCV000144214.3

Allele description [Variation Report for NM_007294.4(BRCA1):c.5407-16C>T]

NM_007294.4(BRCA1):c.5407-16C>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.5407-16C>T
HGVS:
  • NC_000017.11:g.43047719G>A
  • NG_005905.2:g.170265C>T
  • NM_001407571.1:c.5194-16C>T
  • NM_001407581.1:c.5473-16C>T
  • NM_001407582.1:c.5473-16C>T
  • NM_001407583.1:c.5470-16C>T
  • NM_001407585.1:c.5470-16C>T
  • NM_001407587.1:c.5470-16C>T
  • NM_001407590.1:c.5467-16C>T
  • NM_001407591.1:c.5467-16C>T
  • NM_001407593.1:c.5407-16C>T
  • NM_001407594.1:c.5407-16C>T
  • NM_001407596.1:c.5407-16C>T
  • NM_001407597.1:c.5407-16C>T
  • NM_001407598.1:c.5407-16C>T
  • NM_001407602.1:c.5407-16C>T
  • NM_001407603.1:c.5407-16C>T
  • NM_001407605.1:c.5407-16C>T
  • NM_001407610.1:c.5404-16C>T
  • NM_001407611.1:c.5404-16C>T
  • NM_001407612.1:c.5404-16C>T
  • NM_001407613.1:c.5404-16C>T
  • NM_001407614.1:c.5404-16C>T
  • NM_001407615.1:c.5404-16C>T
  • NM_001407616.1:c.5404-16C>T
  • NM_001407617.1:c.5404-16C>T
  • NM_001407618.1:c.5404-16C>T
  • NM_001407619.1:c.5404-16C>T
  • NM_001407620.1:c.5404-16C>T
  • NM_001407621.1:c.5404-16C>T
  • NM_001407622.1:c.5404-16C>T
  • NM_001407623.1:c.5404-16C>T
  • NM_001407624.1:c.5404-16C>T
  • NM_001407625.1:c.5404-16C>T
  • NM_001407626.1:c.5404-16C>T
  • NM_001407627.1:c.5401-16C>T
  • NM_001407628.1:c.5401-16C>T
  • NM_001407629.1:c.5401-16C>T
  • NM_001407630.1:c.5401-16C>T
  • NM_001407631.1:c.5401-16C>T
  • NM_001407632.1:c.5401-16C>T
  • NM_001407633.1:c.5401-16C>T
  • NM_001407634.1:c.5401-16C>T
  • NM_001407635.1:c.5401-16C>T
  • NM_001407636.1:c.5401-16C>T
  • NM_001407637.1:c.5401-16C>T
  • NM_001407638.1:c.5401-16C>T
  • NM_001407639.1:c.5401-16C>T
  • NM_001407640.1:c.5401-16C>T
  • NM_001407641.1:c.5401-16C>T
  • NM_001407642.1:c.5401-16C>T
  • NM_001407644.1:c.5398-16C>T
  • NM_001407645.1:c.5398-16C>T
  • NM_001407646.1:c.5395-16C>T
  • NM_001407647.1:c.5392-16C>T
  • NM_001407648.1:c.5350-16C>T
  • NM_001407649.1:c.5347-16C>T
  • NM_001407652.1:c.5329-16C>T
  • NM_001407653.1:c.5329-16C>T
  • NM_001407654.1:c.5329-16C>T
  • NM_001407655.1:c.5329-16C>T
  • NM_001407656.1:c.5326-16C>T
  • NM_001407657.1:c.5326-16C>T
  • NM_001407658.1:c.5326-16C>T
  • NM_001407659.1:c.5323-16C>T
  • NM_001407660.1:c.5323-16C>T
  • NM_001407661.1:c.5323-16C>T
  • NM_001407662.1:c.5323-16C>T
  • NM_001407663.1:c.5323-16C>T
  • NM_001407664.1:c.5284-16C>T
  • NM_001407665.1:c.5284-16C>T
  • NM_001407666.1:c.5284-16C>T
  • NM_001407667.1:c.5284-16C>T
  • NM_001407668.1:c.5284-16C>T
  • NM_001407669.1:c.5284-16C>T
  • NM_001407670.1:c.5281-16C>T
  • NM_001407671.1:c.5281-16C>T
  • NM_001407672.1:c.5281-16C>T
  • NM_001407673.1:c.5281-16C>T
  • NM_001407674.1:c.5281-16C>T
  • NM_001407675.1:c.5281-16C>T
  • NM_001407676.1:c.5281-16C>T
  • NM_001407677.1:c.5281-16C>T
  • NM_001407678.1:c.5281-16C>T
  • NM_001407679.1:c.5281-16C>T
  • NM_001407680.1:c.5281-16C>T
  • NM_001407681.1:c.5278-16C>T
  • NM_001407682.1:c.5278-16C>T
  • NM_001407683.1:c.5278-16C>T
  • NM_001407684.1:c.5278-16C>T
  • NM_001407685.1:c.5278-16C>T
  • NM_001407686.1:c.5278-16C>T
  • NM_001407687.1:c.5278-16C>T
  • NM_001407688.1:c.5278-16C>T
  • NM_001407689.1:c.5278-16C>T
  • NM_001407690.1:c.5275-16C>T
  • NM_001407691.1:c.5275-16C>T
  • NM_001407692.1:c.5266-16C>T
  • NM_001407694.1:c.5266-16C>T
  • NM_001407695.1:c.5266-16C>T
  • NM_001407696.1:c.5266-16C>T
  • NM_001407697.1:c.5266-16C>T
  • NM_001407698.1:c.5266-16C>T
  • NM_001407724.1:c.5266-16C>T
  • NM_001407725.1:c.5266-16C>T
  • NM_001407726.1:c.5266-16C>T
  • NM_001407727.1:c.5266-16C>T
  • NM_001407728.1:c.5266-16C>T
  • NM_001407729.1:c.5266-16C>T
  • NM_001407730.1:c.5266-16C>T
  • NM_001407731.1:c.5266-16C>T
  • NM_001407732.1:c.5263-16C>T
  • NM_001407733.1:c.5263-16C>T
  • NM_001407734.1:c.5263-16C>T
  • NM_001407735.1:c.5263-16C>T
  • NM_001407736.1:c.5263-16C>T
  • NM_001407737.1:c.5263-16C>T
  • NM_001407738.1:c.5263-16C>T
  • NM_001407739.1:c.5263-16C>T
  • NM_001407740.1:c.5263-16C>T
  • NM_001407741.1:c.5263-16C>T
  • NM_001407742.1:c.5263-16C>T
  • NM_001407743.1:c.5263-16C>T
  • NM_001407744.1:c.5263-16C>T
  • NM_001407745.1:c.5263-16C>T
  • NM_001407746.1:c.5263-16C>T
  • NM_001407747.1:c.5263-16C>T
  • NM_001407748.1:c.5263-16C>T
  • NM_001407749.1:c.5263-16C>T
  • NM_001407750.1:c.5263-16C>T
  • NM_001407751.1:c.5263-16C>T
  • NM_001407752.1:c.5263-16C>T
  • NM_001407838.1:c.5260-16C>T
  • NM_001407839.1:c.5260-16C>T
  • NM_001407841.1:c.5260-16C>T
  • NM_001407842.1:c.5260-16C>T
  • NM_001407843.1:c.5260-16C>T
  • NM_001407844.1:c.5260-16C>T
  • NM_001407845.1:c.5260-16C>T
  • NM_001407846.1:c.5260-16C>T
  • NM_001407847.1:c.5260-16C>T
  • NM_001407848.1:c.5260-16C>T
  • NM_001407849.1:c.5260-16C>T
  • NM_001407850.1:c.5260-16C>T
  • NM_001407851.1:c.5260-16C>T
  • NM_001407852.1:c.5260-16C>T
  • NM_001407853.1:c.5260-16C>T
  • NM_001407854.1:c.5333-16C>T
  • NM_001407858.1:c.5330-16C>T
  • NM_001407859.1:c.5330-16C>T
  • NM_001407860.1:c.5330-16C>T
  • NM_001407861.1:c.5327-16C>T
  • NM_001407862.1:c.5206-16C>T
  • NM_001407863.1:c.5203-16C>T
  • NM_001407874.1:c.5200-16C>T
  • NM_001407875.1:c.5200-16C>T
  • NM_001407879.1:c.5197-16C>T
  • NM_001407881.1:c.5197-16C>T
  • NM_001407882.1:c.5197-16C>T
  • NM_001407884.1:c.5197-16C>T
  • NM_001407885.1:c.5197-16C>T
  • NM_001407886.1:c.5197-16C>T
  • NM_001407887.1:c.5197-16C>T
  • NM_001407889.1:c.5197-16C>T
  • NM_001407894.1:c.5194-16C>T
  • NM_001407895.1:c.5194-16C>T
  • NM_001407896.1:c.5194-16C>T
  • NM_001407897.1:c.5194-16C>T
  • NM_001407898.1:c.5194-16C>T
  • NM_001407899.1:c.5194-16C>T
  • NM_001407900.1:c.5194-16C>T
  • NM_001407902.1:c.5194-16C>T
  • NM_001407904.1:c.5194-16C>T
  • NM_001407906.1:c.5194-16C>T
  • NM_001407907.1:c.5194-16C>T
  • NM_001407908.1:c.5194-16C>T
  • NM_001407909.1:c.5194-16C>T
  • NM_001407910.1:c.5194-16C>T
  • NM_001407915.1:c.5191-16C>T
  • NM_001407916.1:c.5191-16C>T
  • NM_001407917.1:c.5191-16C>T
  • NM_001407918.1:c.5191-16C>T
  • NM_001407919.1:c.5155-16C>T
  • NM_001407920.1:c.5143-16C>T
  • NM_001407921.1:c.5143-16C>T
  • NM_001407922.1:c.5143-16C>T
  • NM_001407923.1:c.5143-16C>T
  • NM_001407924.1:c.5143-16C>T
  • NM_001407925.1:c.5143-16C>T
  • NM_001407926.1:c.5143-16C>T
  • NM_001407927.1:c.5140-16C>T
  • NM_001407928.1:c.5140-16C>T
  • NM_001407929.1:c.5140-16C>T
  • NM_001407930.1:c.5140-16C>T
  • NM_001407931.1:c.5140-16C>T
  • NM_001407932.1:c.5140-16C>T
  • NM_001407933.1:c.5140-16C>T
  • NM_001407934.1:c.5137-16C>T
  • NM_001407935.1:c.5137-16C>T
  • NM_001407936.1:c.5137-16C>T
  • NM_001407937.1:c.5210-16C>T
  • NM_001407938.1:c.5210-16C>T
  • NM_001407939.1:c.5207-16C>T
  • NM_001407940.1:c.5207-16C>T
  • NM_001407941.1:c.5204-16C>T
  • NM_001407942.1:c.5192-16C>T
  • NM_001407943.1:c.5189-16C>T
  • NM_001407944.1:c.5189-16C>T
  • NM_001407945.1:c.5189-16C>T
  • NM_001407946.1:c.5074-16C>T
  • NM_001407947.1:c.5074-16C>T
  • NM_001407948.1:c.5074-16C>T
  • NM_001407949.1:c.5074-16C>T
  • NM_001407950.1:c.5071-16C>T
  • NM_001407951.1:c.5071-16C>T
  • NM_001407952.1:c.5071-16C>T
  • NM_001407953.1:c.5071-16C>T
  • NM_001407954.1:c.5071-16C>T
  • NM_001407955.1:c.5071-16C>T
  • NM_001407956.1:c.5068-16C>T
  • NM_001407957.1:c.5068-16C>T
  • NM_001407958.1:c.5068-16C>T
  • NM_001407959.1:c.5026-16C>T
  • NM_001407960.1:c.5023-16C>T
  • NM_001407962.1:c.5023-16C>T
  • NM_001407963.1:c.5020-16C>T
  • NM_001407964.1:c.4945-16C>T
  • NM_001407965.1:c.4900-16C>T
  • NM_001407966.1:c.4519-16C>T
  • NM_001407967.1:c.4516-16C>T
  • NM_001407968.1:c.2803-16C>T
  • NM_001407969.1:c.2800-16C>T
  • NM_001407970.1:c.2164-16C>T
  • NM_001407971.1:c.2164-16C>T
  • NM_001407972.1:c.2161-16C>T
  • NM_001407973.1:c.2098-16C>T
  • NM_001407974.1:c.2098-16C>T
  • NM_001407975.1:c.2098-16C>T
  • NM_001407976.1:c.2098-16C>T
  • NM_001407977.1:c.2098-16C>T
  • NM_001407978.1:c.2098-16C>T
  • NM_001407979.1:c.2095-16C>T
  • NM_001407980.1:c.2095-16C>T
  • NM_001407981.1:c.2095-16C>T
  • NM_001407982.1:c.2095-16C>T
  • NM_001407983.1:c.2095-16C>T
  • NM_001407984.1:c.2095-16C>T
  • NM_001407985.1:c.2095-16C>T
  • NM_001407986.1:c.2095-16C>T
  • NM_001407990.1:c.2095-16C>T
  • NM_001407991.1:c.2095-16C>T
  • NM_001407992.1:c.2095-16C>T
  • NM_001407993.1:c.2095-16C>T
  • NM_001408392.1:c.2092-16C>T
  • NM_001408396.1:c.2092-16C>T
  • NM_001408397.1:c.2092-16C>T
  • NM_001408398.1:c.2092-16C>T
  • NM_001408399.1:c.2092-16C>T
  • NM_001408400.1:c.2092-16C>T
  • NM_001408401.1:c.2092-16C>T
  • NM_001408402.1:c.2092-16C>T
  • NM_001408403.1:c.2092-16C>T
  • NM_001408404.1:c.2092-16C>T
  • NM_001408406.1:c.2089-16C>T
  • NM_001408407.1:c.2089-16C>T
  • NM_001408408.1:c.2089-16C>T
  • NM_001408409.1:c.2086-16C>T
  • NM_001408410.1:c.2023-16C>T
  • NM_001408411.1:c.2020-16C>T
  • NM_001408412.1:c.2017-16C>T
  • NM_001408413.1:c.2017-16C>T
  • NM_001408414.1:c.2017-16C>T
  • NM_001408415.1:c.2017-16C>T
  • NM_001408416.1:c.2017-16C>T
  • NM_001408418.1:c.1981-16C>T
  • NM_001408419.1:c.1981-16C>T
  • NM_001408420.1:c.1981-16C>T
  • NM_001408421.1:c.1978-16C>T
  • NM_001408422.1:c.1978-16C>T
  • NM_001408423.1:c.1978-16C>T
  • NM_001408424.1:c.1978-16C>T
  • NM_001408425.1:c.1975-16C>T
  • NM_001408426.1:c.1975-16C>T
  • NM_001408427.1:c.1975-16C>T
  • NM_001408428.1:c.1975-16C>T
  • NM_001408429.1:c.1975-16C>T
  • NM_001408430.1:c.1975-16C>T
  • NM_001408431.1:c.1975-16C>T
  • NM_001408432.1:c.1972-16C>T
  • NM_001408433.1:c.1972-16C>T
  • NM_001408434.1:c.1972-16C>T
  • NM_001408435.1:c.1972-16C>T
  • NM_001408436.1:c.1972-16C>T
  • NM_001408437.1:c.1972-16C>T
  • NM_001408438.1:c.1972-16C>T
  • NM_001408439.1:c.1972-16C>T
  • NM_001408440.1:c.1972-16C>T
  • NM_001408441.1:c.1972-16C>T
  • NM_001408442.1:c.1972-16C>T
  • NM_001408443.1:c.1972-16C>T
  • NM_001408444.1:c.1972-16C>T
  • NM_001408445.1:c.1969-16C>T
  • NM_001408446.1:c.1969-16C>T
  • NM_001408447.1:c.1969-16C>T
  • NM_001408448.1:c.1969-16C>T
  • NM_001408450.1:c.1969-16C>T
  • NM_001408451.1:c.1963-16C>T
  • NM_001408452.1:c.1957-16C>T
  • NM_001408453.1:c.1957-16C>T
  • NM_001408454.1:c.1957-16C>T
  • NM_001408455.1:c.1957-16C>T
  • NM_001408456.1:c.1957-16C>T
  • NM_001408457.1:c.1957-16C>T
  • NM_001408458.1:c.1954-16C>T
  • NM_001408459.1:c.1954-16C>T
  • NM_001408460.1:c.1954-16C>T
  • NM_001408461.1:c.1954-16C>T
  • NM_001408462.1:c.1954-16C>T
  • NM_001408463.1:c.1954-16C>T
  • NM_001408464.1:c.1954-16C>T
  • NM_001408465.1:c.1954-16C>T
  • NM_001408466.1:c.1954-16C>T
  • NM_001408467.1:c.1954-16C>T
  • NM_001408468.1:c.1951-16C>T
  • NM_001408469.1:c.1951-16C>T
  • NM_001408470.1:c.1951-16C>T
  • NM_001408472.1:c.2021-16C>T
  • NM_001408473.1:c.2018-16C>T
  • NM_001408474.1:c.1897-16C>T
  • NM_001408475.1:c.1894-16C>T
  • NM_001408476.1:c.1894-16C>T
  • NM_001408478.1:c.1888-16C>T
  • NM_001408479.1:c.1888-16C>T
  • NM_001408480.1:c.1888-16C>T
  • NM_001408481.1:c.1885-16C>T
  • NM_001408482.1:c.1885-16C>T
  • NM_001408483.1:c.1885-16C>T
  • NM_001408484.1:c.1885-16C>T
  • NM_001408485.1:c.1885-16C>T
  • NM_001408489.1:c.1885-16C>T
  • NM_001408490.1:c.1885-16C>T
  • NM_001408491.1:c.1885-16C>T
  • NM_001408492.1:c.1882-16C>T
  • NM_001408493.1:c.1882-16C>T
  • NM_001408494.1:c.1858-16C>T
  • NM_001408495.1:c.1852-16C>T
  • NM_001408496.1:c.1834-16C>T
  • NM_001408497.1:c.1834-16C>T
  • NM_001408498.1:c.1834-16C>T
  • NM_001408499.1:c.1834-16C>T
  • NM_001408500.1:c.1834-16C>T
  • NM_001408501.1:c.1834-16C>T
  • NM_001408502.1:c.1831-16C>T
  • NM_001408503.1:c.1831-16C>T
  • NM_001408504.1:c.1831-16C>T
  • NM_001408505.1:c.1828-16C>T
  • NM_001408506.1:c.1771-16C>T
  • NM_001408507.1:c.1768-16C>T
  • NM_001408508.1:c.1759-16C>T
  • NM_001408509.1:c.1756-16C>T
  • NM_001408510.1:c.1717-16C>T
  • NM_001408511.1:c.1714-16C>T
  • NM_001408512.1:c.1594-16C>T
  • NM_001408513.1:c.1567-16C>T
  • NM_001408514.1:c.1171-16C>T
  • NM_007294.4:c.5407-16C>TMANE SELECT
  • NM_007297.4:c.5266-16C>T
  • NM_007298.4:c.2095-16C>T
  • NM_007299.4:c.2021-16C>T
  • NM_007300.4:c.5470-16C>T
  • LRG_292t1:c.5407-16C>T
  • LRG_292:g.170265C>T
  • NC_000017.10:g.41199736G>A
  • NM_007294.3:c.5407-16C>T
Nucleotide change:
IVS22-16C>T
Links:
dbSNP: rs587776493
NCBI 1000 Genomes Browser:
rs587776493
Molecular consequence:
  • NM_001407571.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407581.1:c.5473-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407582.1:c.5473-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407583.1:c.5470-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407585.1:c.5470-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407587.1:c.5470-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407590.1:c.5467-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407591.1:c.5467-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407593.1:c.5407-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407594.1:c.5407-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407596.1:c.5407-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407597.1:c.5407-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407598.1:c.5407-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407602.1:c.5407-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407603.1:c.5407-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407605.1:c.5407-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407610.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407611.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407612.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407613.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407614.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407615.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407616.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407617.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407618.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407619.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407620.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407621.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407622.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407623.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407624.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407625.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407626.1:c.5404-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407627.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407628.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407629.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407630.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407631.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407632.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407633.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407634.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407635.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407636.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407637.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407638.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407639.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407640.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407641.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407642.1:c.5401-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407644.1:c.5398-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407645.1:c.5398-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407646.1:c.5395-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407647.1:c.5392-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407648.1:c.5350-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407649.1:c.5347-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407652.1:c.5329-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407653.1:c.5329-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407654.1:c.5329-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407655.1:c.5329-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407656.1:c.5326-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407657.1:c.5326-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407658.1:c.5326-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407659.1:c.5323-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407660.1:c.5323-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407661.1:c.5323-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407662.1:c.5323-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407663.1:c.5323-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407664.1:c.5284-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407665.1:c.5284-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407666.1:c.5284-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407667.1:c.5284-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407668.1:c.5284-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407669.1:c.5284-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407670.1:c.5281-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407671.1:c.5281-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407672.1:c.5281-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407673.1:c.5281-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407674.1:c.5281-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407675.1:c.5281-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407676.1:c.5281-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407677.1:c.5281-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407678.1:c.5281-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407679.1:c.5281-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407680.1:c.5281-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407681.1:c.5278-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407682.1:c.5278-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407683.1:c.5278-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407684.1:c.5278-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407685.1:c.5278-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407686.1:c.5278-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407687.1:c.5278-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407688.1:c.5278-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407689.1:c.5278-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407690.1:c.5275-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407691.1:c.5275-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407692.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407694.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407695.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407696.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407697.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407698.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407724.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407725.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407726.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407727.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407728.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407729.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407730.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407731.1:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407732.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407733.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407734.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407735.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407736.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407737.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407738.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407739.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407740.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407741.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407742.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407743.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407744.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407745.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407746.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407747.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407748.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407749.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407750.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407751.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407752.1:c.5263-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407838.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407839.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407841.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407842.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407843.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407844.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407845.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407846.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407847.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407848.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407849.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407850.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407851.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407852.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407853.1:c.5260-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407854.1:c.5333-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407858.1:c.5330-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407859.1:c.5330-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407860.1:c.5330-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407861.1:c.5327-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407862.1:c.5206-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407863.1:c.5203-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407874.1:c.5200-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407875.1:c.5200-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407879.1:c.5197-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407881.1:c.5197-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407882.1:c.5197-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407884.1:c.5197-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407885.1:c.5197-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407886.1:c.5197-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407887.1:c.5197-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407889.1:c.5197-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407894.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407895.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407896.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407897.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407898.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407899.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407900.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407902.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407904.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407906.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407907.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407908.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407909.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407910.1:c.5194-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407915.1:c.5191-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407916.1:c.5191-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407917.1:c.5191-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407918.1:c.5191-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407919.1:c.5155-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407920.1:c.5143-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407921.1:c.5143-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407922.1:c.5143-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407923.1:c.5143-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407924.1:c.5143-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407925.1:c.5143-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407926.1:c.5143-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407927.1:c.5140-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407928.1:c.5140-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407929.1:c.5140-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407930.1:c.5140-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407931.1:c.5140-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407932.1:c.5140-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407933.1:c.5140-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407934.1:c.5137-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407935.1:c.5137-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407936.1:c.5137-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407937.1:c.5210-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407938.1:c.5210-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407939.1:c.5207-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407940.1:c.5207-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407941.1:c.5204-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407942.1:c.5192-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407943.1:c.5189-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407944.1:c.5189-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407945.1:c.5189-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407946.1:c.5074-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407947.1:c.5074-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407948.1:c.5074-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407949.1:c.5074-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407950.1:c.5071-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407951.1:c.5071-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407952.1:c.5071-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407953.1:c.5071-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407954.1:c.5071-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407955.1:c.5071-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407956.1:c.5068-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407957.1:c.5068-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407958.1:c.5068-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407959.1:c.5026-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407960.1:c.5023-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407962.1:c.5023-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407963.1:c.5020-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407964.1:c.4945-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407965.1:c.4900-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407966.1:c.4519-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407967.1:c.4516-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407968.1:c.2803-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407969.1:c.2800-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407970.1:c.2164-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.2164-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.2161-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.2098-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.2098-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.2098-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.2098-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.2098-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.2098-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.2092-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.2092-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.2092-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.2092-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.2092-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.2092-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.2092-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.2092-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.2092-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.2092-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.2089-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.2089-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.2089-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.2086-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.2023-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.2020-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.2017-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.2017-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.2017-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.2017-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.2017-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.1981-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.1981-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.1981-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.1978-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.1978-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.1978-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.1978-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.1975-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.1975-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.1975-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.1975-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.1975-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.1975-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.1975-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.1972-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.1969-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.1969-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.1969-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.1969-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.1969-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.1963-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.1957-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.1957-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.1957-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.1957-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.1957-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.1957-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.1954-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.1954-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.1954-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.1954-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.1954-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.1954-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.1954-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.1954-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.1954-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.1954-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.1951-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.1951-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.1951-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.2021-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.2018-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.1897-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.1894-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.1894-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.1888-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.1888-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.1888-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.1885-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.1885-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.1885-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.1885-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.1885-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.1885-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.1885-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.1885-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.1882-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.1882-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.1858-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.1852-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.1834-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.1834-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.1834-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.1834-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.1834-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.1834-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.1831-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.1831-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.1831-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.1828-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.1771-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.1768-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.1759-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.1756-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.1717-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.1714-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.1594-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.1567-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.1171-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007294.4:c.5407-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007297.4:c.5266-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.2095-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.2021-16C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007300.4:c.5470-16C>T - intron variant - [Sequence Ontology: SO:0001627]
Observations:
1

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

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000189287Sharing Clinical Reports Project (SCRP)
no assertion criteria provided
Likely benign
(Feb 25, 2011) 		germlineclinical testing

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot provided1not providednot provided1not providedclinical testing

Details of each submission

From Sharing Clinical Reports Project (SCRP), SCV000189287.1

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

Last Updated: Oct 8, 2024