Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.43041660_43046086delinsCTGTG | CA2580093779 | ClinVar | ||
17 | g.43041662_43046087delinsTG | CA16043342 | ClinVar | ||
17 | g.43044295_43045802del | CA915950020 | ClinVar | ||
17 | g.43044924_43051621del | CA2580093785 | BRCA1 | c.5275-502_*756del c.5278-502_*756del c.5152-502_*756del c.5272-502_*756del c.5200-502_*756del c.1966-502_*756del c.1828-502_*756del c.4390-502_*756del c.5155-502_*756del c.5137-502_*756del c.5341-502_*756del c.1852-502_*756del c.1966-502_*862del n.5414-502_6484del n.5455-502_6525del | ClinVar |
17 | g.43045093_43046211del | CA2697559962 | BRCA1 | c.5465-364_*630del c.5468-364_*630del c.5342-364_*630del c.5462-364_*630del c.5390-364_*630del c.2156-364_*630del c.2018-364_*630del c.4580-364_*630del c.5345-364_*630del c.5327-364_*630del n.1351-364_2105del n.832-364_1586del c.5531-364_*630del c.2042-364_*630del c.2082-364_*736del n.5604-364_6358del n.5645-364_6399del | ClinVar |
17 | g.43045329_43045805del | CA2581463415 | BRCA1 | c.5465_*352del c.5468_*352del c.5342_*352del c.5462_*352del c.5390_*352del c.2156_*352del c.2018_*352del c.4580_*352del c.5345_*352del c.5534_*352del c.5327_*352del n.1351_1827del n.832_1308del c.5531_*352del c.1855_2331del c.2042_*352del c.2082_*458del n.5604_6080del n.5645_6121del | |
17 | g.43045658_43051137del | CA915940399 | BRCA1 | c.5275-20_*20del c.5278-20_*20del c.5152-20_*20del c.5272-20_*20del c.5200-20_*20del c.1966-20_*20del c.1828-20_*20del c.4390-20_*20del c.5155-20_*20del c.5344-20_*20del c.5137-20_*20del c.1840-20_*20del c.5341-20_*20del c.1665-20_1999del c.1852-20_*20del c.1966-20_*126del c.208-20_*20del c.751-20_*20del c.-98-947_*20del n.5414-20_5748del n.5455-20_5789del | |
17 | g.43045676_43045803del | CA2499224337 | BRCA1 | c.5467_*5del c.5470_*5del c.5344_*5del c.5464_*5del c.5392_*5del c.2158_*5del c.2020_*5del c.4582_*5del c.5347_*5del c.5536_*5del c.5329_*5del c.2032_*5del n.1353_1480del n.834_961del c.5533_*5del c.1857_1984del c.2044_*5del c.2084_*111del c.400_*5del c.943_*5del c.169_*5del n.5606_5733del n.5647_5774del | ClinVar dbSNP |
17 | g.43045676_43045993del | CA2499224338 | BRCA1 | c.5465-191_*2del c.5468-191_*2del c.5342-191_*2del c.5462-191_*2del c.5390-191_*2del c.2156-191_*2del c.2018-191_*2del c.4580-191_*2del c.5345-191_*2del c.5534-191_*2del c.5327-191_*2del c.2030-191_*2del n.1351-191_1477del n.832-191_958del c.5531-191_*2del c.1855-191_1981del c.2042-191_*2del c.2082-191_*108del c.398-191_*2del c.941-191_*2del c.167-191_*2del n.5604-191_5730del n.5645-191_5771del | ClinVar dbSNP |
17 | g.43045678_43047703del | CA2581463416 | BRCA1 | c.5404_5589del c.5407_5592del c.5281_5466del c.5401_5586del c.5329_5514del c.2095_2280del c.1957_2142del c.4519_4704del c.5284_5469del c.5473_5658del c.5266_5451del c.1969_2154del n.1290_1475del n.771_956del c.5470_5655del c.1794_1979del c.1981_2166del c.*5190_*5375del c.2021_*106del c.337_522del c.880_1065del c.106_291del n.5543_5728del n.5584_5769del | |
17 | g.43045678_43051117del | CA2581463401 | BRCA1 | c.5275_5589del c.5278_5592del c.5152_5466del c.5272_5586del c.5200_5514del c.1966_2280del c.1828_2142del c.4390_4704del c.5155_5469del c.5344_5658del c.5137_5451del c.1840_2154del c.5341_5655del c.1665_1979del c.1852_2166del c.*5061_*5375del c.1966_*106del c.208_522del c.751_1065del c.-98-927_291del n.5414_5728del n.5455_5769del | |
17 | g.43045705_43045767delinsTATCAGGTAGGTGTCCAGCTCCTGGCACTGGTAGAGTGCTACACTGTCCAACACCCACTCTCG | CA2260761028 | BRCA1 | c.5500_5562delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg1834=) c.5503_5565delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg1835=) c.5377_5439delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg1793=) c.5497_5559delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg1833=) c.5425_5487delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg1809=) c.2191_2253delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg731=) c.2053_2115delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg685=) c.4615_4677delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg1539=) c.5380_5442delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg1794=) c.5569_5631delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg1857=) c.5362_5424delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg1788=) c.2065_2127delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg689=) n.1386_1448delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA n.867_929delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA c.5566_5628delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg1856=) c.1890_1952delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA c.2077_2139delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg693=) c.*5286_*5348delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (n.*5286_*5348delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA) c.*17_*79delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (n.*17_*79delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA) c.433_495delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg145=) c.976_1038delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg326=) c.202_264delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA (p.Arg68=) n.5639_5701delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA n.5680_5742delinsCGAGAGTGGGTGTTGGACAGTGTAGCACTCTACCAGTGCCAGGAGCTGGACACCTACCTGATA | |
17 | g.43045706_43045767del | CA003672 | BRCA1 | c.5500_5561del (p.Arg1834ThrfsTer24) c.5503_5564del (p.Arg1835ThrfsTer24) c.5377_5438del (p.Arg1793ThrfsTer24) c.5497_5558del (p.Arg1833ThrfsTer24) c.5425_5486del (p.Arg1809ThrfsTer24) c.2191_2252del (p.Arg731ThrfsTer24) c.2053_2114del (p.Arg685ThrfsTer24) c.4615_4676del (p.Arg1539ThrfsTer24) c.5380_5441del (p.Arg1794ThrfsTer24) c.5569_5630del (p.Arg1857ThrfsTer24) c.5362_5423del (p.Arg1788ThrfsTer24) c.2065_2126del (p.Arg689ThrfsTer24) n.1386_1447del n.867_928del c.5566_5627del (p.Arg1856ThrfsTer24) c.1890_1951del c.2077_2138del (p.Arg693ThrfsTer24) c.*5286_*5347del (n.*5286_*5347del) c.*17_*78del (n.*17_*78del) c.2191_2252del (p.Arg731ThrfsTer?) c.433_494del (p.Arg145ThrfsTer24) c.976_1037del (p.Arg326ThrfsTer24) c.202_263del (p.Arg68ThrfsTer24) n.5639_5700del n.5680_5741del | ClinVar dbSNP |
17 | g.43045713_43045733delinsAGGTGTCCAGCTCCTGGCACT | CA2260761043 | BRCA1 | c.5534_5554delinsAGTGCCAGGAGCTGGACACCT (p.Gln1845=) c.5537_5557delinsAGTGCCAGGAGCTGGACACCT (p.Gln1846=) c.5411_5431delinsAGTGCCAGGAGCTGGACACCT (p.Gln1804=) c.5531_5551delinsAGTGCCAGGAGCTGGACACCT (p.Gln1844=) c.5459_5479delinsAGTGCCAGGAGCTGGACACCT (p.Gln1820=) c.2225_2245delinsAGTGCCAGGAGCTGGACACCT (p.Gln742=) c.2087_2107delinsAGTGCCAGGAGCTGGACACCT (p.Gln696=) c.4649_4669delinsAGTGCCAGGAGCTGGACACCT (p.Gln1550=) c.5414_5434delinsAGTGCCAGGAGCTGGACACCT (p.Gln1805=) c.5603_5623delinsAGTGCCAGGAGCTGGACACCT (p.Gln1868=) c.5396_5416delinsAGTGCCAGGAGCTGGACACCT (p.Gln1799=) c.2099_2119delinsAGTGCCAGGAGCTGGACACCT (p.Gln700=) n.1420_1440delinsAGTGCCAGGAGCTGGACACCT n.901_921delinsAGTGCCAGGAGCTGGACACCT c.5600_5620delinsAGTGCCAGGAGCTGGACACCT (p.Gln1867=) c.1924_1944delinsAGTGCCAGGAGCTGGACACCT c.2111_2131delinsAGTGCCAGGAGCTGGACACCT (p.Gln704=) c.*5320_*5340delinsAGTGCCAGGAGCTGGACACCT (n.*5320_*5340delinsAGTGCCAGGAGCTGGACACCT) c.*51_*71delinsAGTGCCAGGAGCTGGACACCT (n.*51_*71delinsAGTGCCAGGAGCTGGACACCT) c.467_487delinsAGTGCCAGGAGCTGGACACCT (p.Gln156=) c.1010_1030delinsAGTGCCAGGAGCTGGACACCT (p.Gln337=) c.236_256delinsAGTGCCAGGAGCTGGACACCT (p.Gln79=) n.5673_5693delinsAGTGCCAGGAGCTGGACACCT n.5714_5734delinsAGTGCCAGGAGCTGGACACCT | |
17 | g.43045717_43045736del | CA10589581 | BRCA1 | c.5534_5553del (p.Gln1845LeufsTer27) c.5537_5556del (p.Gln1846LeufsTer27) c.5411_5430del (p.Gln1804LeufsTer27) c.5531_5550del (p.Gln1844LeufsTer27) c.5459_5478del (p.Gln1820LeufsTer27) c.2225_2244del (p.Gln742LeufsTer27) c.2087_2106del (p.Gln696LeufsTer27) c.4649_4668del (p.Gln1550LeufsTer27) c.5414_5433del (p.Gln1805LeufsTer27) c.5603_5622del (p.Gln1868LeufsTer27) c.5396_5415del (p.Gln1799LeufsTer27) c.2099_2118del (p.Gln700LeufsTer27) n.1420_1439del n.901_920del c.5600_5619del (p.Gln1867LeufsTer27) c.1924_1943del c.2111_2130del (p.Gln704LeufsTer27) c.*5320_*5339del (n.*5320_*5339del) c.*51_*70del (n.*51_*70del) c.2225_2244del (p.Gln742LeufsTer?) c.467_486del (p.Gln156LeufsTer27) c.1010_1029del (p.Gln337LeufsTer27) c.236_255del (p.Gln79LeufsTer27) n.5673_5692del n.5714_5733del | ClinVar dbSNP |
17 | g.43045717_43045718del | CA916080701 | BRCA1 | c.5551_5552del (p.Thr1851LeufsTer27) c.5554_5555del (p.Thr1852LeufsTer27) c.5428_5429del (p.Thr1810LeufsTer27) c.5548_5549del (p.Thr1850LeufsTer27) c.5476_5477del (p.Thr1826LeufsTer27) c.2242_2243del (p.Thr748LeufsTer27) c.2104_2105del (p.Thr702LeufsTer27) c.4666_4667del (p.Thr1556LeufsTer27) c.5431_5432del (p.Thr1811LeufsTer27) c.5620_5621del (p.Thr1874LeufsTer27) c.5413_5414del (p.Thr1805LeufsTer27) c.2116_2117del (p.Thr706LeufsTer27) n.1437_1438del n.918_919del c.5617_5618del (p.Thr1873LeufsTer27) c.1941_1942del c.2128_2129del (p.Thr710LeufsTer27) c.*5337_*5338del (n.*5337_*5338del) c.*68_*69del (n.*68_*69del) c.2242_2243del (p.Thr748LeufsTer?) c.484_485del (p.Thr162LeufsTer27) c.1027_1028del (p.Thr343LeufsTer27) c.253_254del (p.Thr85LeufsTer27) n.5690_5691del n.5731_5732del | ClinVar dbSNP |
17 | g.43045718T>A | CA10590215 | BRCA1 | c.5549A>T (p.Asp1850Val) c.5552A>T (p.Asp1851Val) c.5426A>T (p.Asp1809Val) c.5546A>T (p.Asp1849Val) c.5474A>T (p.Asp1825Val) c.2240A>T (p.Asp747Val) c.2102A>T (p.Asp701Val) c.4664A>T (p.Asp1555Val) c.5429A>T (p.Asp1810Val) c.5618A>T (p.Asp1873Val) c.5411A>T (p.Asp1804Val) c.2114A>T (p.Asp705Val) n.1435A>T n.916A>T c.5615A>T (p.Asp1872Val) c.1939A>T c.2126A>T (p.Asp709Val) c.*5335A>T (n.*5335A>T) c.*66A>T (n.*66A>T) c.482A>T (p.Asp161Val) c.1025A>T (p.Asp342Val) c.251A>T (p.Asp84Val) n.5688A>T n.5729A>T | ClinVar dbSNP |
17 | g.43045718T>C | CA10590216 | BRCA1 | c.5549A>G (p.Asp1850Gly) c.5552A>G (p.Asp1851Gly) c.5426A>G (p.Asp1809Gly) c.5546A>G (p.Asp1849Gly) c.5474A>G (p.Asp1825Gly) c.2240A>G (p.Asp747Gly) c.2102A>G (p.Asp701Gly) c.4664A>G (p.Asp1555Gly) c.5429A>G (p.Asp1810Gly) c.5618A>G (p.Asp1873Gly) c.5411A>G (p.Asp1804Gly) c.2114A>G (p.Asp705Gly) n.1435A>G n.916A>G c.5615A>G (p.Asp1872Gly) c.1939A>G c.2126A>G (p.Asp709Gly) c.*5335A>G (n.*5335A>G) c.*66A>G (n.*66A>G) c.482A>G (p.Asp161Gly) c.1025A>G (p.Asp342Gly) c.251A>G (p.Asp84Gly) n.5688A>G n.5729A>G | ClinVar dbSNP |
17 | g.43045718T>G | CA10590217 | BRCA1 | c.5549A>C (p.Asp1850Ala) c.5552A>C (p.Asp1851Ala) c.5426A>C (p.Asp1809Ala) c.5546A>C (p.Asp1849Ala) c.5474A>C (p.Asp1825Ala) c.2240A>C (p.Asp747Ala) c.2102A>C (p.Asp701Ala) c.4664A>C (p.Asp1555Ala) c.5429A>C (p.Asp1810Ala) c.5618A>C (p.Asp1873Ala) c.5411A>C (p.Asp1804Ala) c.2114A>C (p.Asp705Ala) n.1435A>C n.916A>C c.5615A>C (p.Asp1872Ala) c.1939A>C c.2126A>C (p.Asp709Ala) c.*5335A>C (n.*5335A>C) c.*66A>C (n.*66A>C) c.482A>C (p.Asp161Ala) c.1025A>C (p.Asp342Ala) c.251A>C (p.Asp84Ala) n.5688A>C n.5729A>C | ClinVar dbSNP |
17 | g.43045718T= | CA2260761051 | BRCA1 | c.5549A= (p.Asp1850=) c.5552A= (p.Asp1851=) c.5426A= (p.Asp1809=) c.5546A= (p.Asp1849=) c.5474A= (p.Asp1825=) c.2240A= (p.Asp747=) c.2102A= (p.Asp701=) c.4664A= (p.Asp1555=) c.5429A= (p.Asp1810=) c.5618A= (p.Asp1873=) c.5411A= (p.Asp1804=) c.2114A= (p.Asp705=) n.1435A= n.916A= c.5615A= (p.Asp1872=) c.1939A= c.2126A= (p.Asp709=) c.*5335A= (n.*5335A=) c.*66A= (n.*66A=) c.482A= (p.Asp161=) c.1025A= (p.Asp342=) c.251A= (p.Asp84=) n.5688A= n.5729A= | |
17 | g.43045718_43045719delinsTC | CA2260761050 | BRCA1 | c.5548_5549delinsGA (p.Asp1850=) c.5551_5552delinsGA (p.Asp1851=) c.5425_5426delinsGA (p.Asp1809=) c.5545_5546delinsGA (p.Asp1849=) c.5473_5474delinsGA (p.Asp1825=) c.2239_2240delinsGA (p.Asp747=) c.2101_2102delinsGA (p.Asp701=) c.4663_4664delinsGA (p.Asp1555=) c.5428_5429delinsGA (p.Asp1810=) c.5617_5618delinsGA (p.Asp1873=) c.5410_5411delinsGA (p.Asp1804=) c.2113_2114delinsGA (p.Asp705=) n.1434_1435delinsGA n.915_916delinsGA c.5614_5615delinsGA (p.Asp1872=) c.1938_1939delinsGA c.2125_2126delinsGA (p.Asp709=) c.*5334_*5335delinsGA (n.*5334_*5335delinsGA) c.*65_*66delinsGA (n.*65_*66delinsGA) c.481_482delinsGA (p.Asp161=) c.1024_1025delinsGA (p.Asp342=) c.250_251delinsGA (p.Asp84=) n.5687_5688delinsGA n.5728_5729delinsGA | |
17 | g.43045719C>A | CA10590218 | BRCA1 | c.5548G>T (p.Asp1850Tyr) c.5551G>T (p.Asp1851Tyr) c.5425G>T (p.Asp1809Tyr) c.5545G>T (p.Asp1849Tyr) c.5473G>T (p.Asp1825Tyr) c.2239G>T (p.Asp747Tyr) c.2101G>T (p.Asp701Tyr) c.4663G>T (p.Asp1555Tyr) c.5428G>T (p.Asp1810Tyr) c.5617G>T (p.Asp1873Tyr) c.5410G>T (p.Asp1804Tyr) c.2113G>T (p.Asp705Tyr) n.1434G>T n.915G>T c.5614G>T (p.Asp1872Tyr) c.1938G>T c.2125G>T (p.Asp709Tyr) c.*5334G>T (n.*5334G>T) c.*65G>T (n.*65G>T) c.481G>T (p.Asp161Tyr) c.1024G>T (p.Asp342Tyr) c.250G>T (p.Asp84Tyr) n.5687G>T n.5728G>T | ClinVar dbSNP |
17 | g.43045719C= | CA2260761052 | BRCA1 | c.5548G= (p.Asp1850=) c.5551G= (p.Asp1851=) c.5425G= (p.Asp1809=) c.5545G= (p.Asp1849=) c.5473G= (p.Asp1825=) c.2239G= (p.Asp747=) c.2101G= (p.Asp701=) c.4663G= (p.Asp1555=) c.5428G= (p.Asp1810=) c.5617G= (p.Asp1873=) c.5410G= (p.Asp1804=) c.2113G= (p.Asp705=) n.1434G= n.915G= c.5614G= (p.Asp1872=) c.1938G= c.2125G= (p.Asp709=) c.*5334G= (n.*5334G=) c.*65G= (n.*65G=) c.481G= (p.Asp161=) c.1024G= (p.Asp342=) c.250G= (p.Asp84=) n.5687G= n.5728G= | |
17 | g.43045719C>G | CA10590219 | BRCA1 | c.5548G>C (p.Asp1850His) c.5551G>C (p.Asp1851His) c.5425G>C (p.Asp1809His) c.5545G>C (p.Asp1849His) c.5473G>C (p.Asp1825His) c.2239G>C (p.Asp747His) c.2101G>C (p.Asp701His) c.4663G>C (p.Asp1555His) c.5428G>C (p.Asp1810His) c.5617G>C (p.Asp1873His) c.5410G>C (p.Asp1804His) c.2113G>C (p.Asp705His) n.1434G>C n.915G>C c.5614G>C (p.Asp1872His) c.1938G>C c.2125G>C (p.Asp709His) c.*5334G>C (n.*5334G>C) c.*65G>C (n.*65G>C) c.481G>C (p.Asp161His) c.1024G>C (p.Asp342His) c.250G>C (p.Asp84His) n.5687G>C n.5728G>C | ClinVar dbSNP |
17 | g.43045719C>T | CA10590220 | BRCA1 | c.5548G>A (p.Asp1850Asn) c.5551G>A (p.Asp1851Asn) c.5425G>A (p.Asp1809Asn) c.5545G>A (p.Asp1849Asn) c.5473G>A (p.Asp1825Asn) c.2239G>A (p.Asp747Asn) c.2101G>A (p.Asp701Asn) c.4663G>A (p.Asp1555Asn) c.5428G>A (p.Asp1810Asn) c.5617G>A (p.Asp1873Asn) c.5410G>A (p.Asp1804Asn) c.2113G>A (p.Asp705Asn) n.1434G>A n.915G>A c.5614G>A (p.Asp1872Asn) c.1938G>A c.2125G>A (p.Asp709Asn) c.*5334G>A (n.*5334G>A) c.*65G>A (n.*65G>A) c.481G>A (p.Asp161Asn) c.1024G>A (p.Asp342Asn) c.250G>A (p.Asp84Asn) n.5687G>A n.5728G>A | ClinVar dbSNP |
17 | g.43045720del | CA10589582 | BRCA1 | c.5548del (p.Asp1850ThrfsTer4) c.5551del (p.Asp1851ThrfsTer4) c.5425del (p.Asp1809ThrfsTer4) c.5545del (p.Asp1849ThrfsTer4) c.5473del (p.Asp1825ThrfsTer4) c.2239del (p.Asp747ThrfsTer4) c.2101del (p.Asp701ThrfsTer4) c.4663del (p.Asp1555ThrfsTer4) c.5428del (p.Asp1810ThrfsTer4) c.5617del (p.Asp1873ThrfsTer4) c.5410del (p.Asp1804ThrfsTer4) c.2113del (p.Asp705ThrfsTer4) n.1434del n.915del c.5614del (p.Asp1872ThrfsTer4) c.1938del c.2125del (p.Asp709ThrfsTer4) c.*5334del (n.*5334del) c.*65del (n.*65del) c.481del (p.Asp161ThrfsTer4) c.1024del (p.Asp342ThrfsTer4) c.250del (p.Asp84ThrfsTer4) n.5687del n.5728del | ClinVar dbSNP |
17 | g.43045720C>A | CA500142886 | BRCA1 | c.5547G>T (p.Leu1849=) c.5550G>T (p.Leu1850=) c.5424G>T (p.Leu1808=) c.5544G>T (p.Leu1848=) c.5472G>T (p.Leu1824=) c.2238G>T (p.Leu746=) c.2100G>T (p.Leu700=) c.4662G>T (p.Leu1554=) c.5427G>T (p.Leu1809=) c.5616G>T (p.Leu1872=) c.5409G>T (p.Leu1803=) c.2112G>T (p.Leu704=) n.1433G>T n.914G>T c.5613G>T (p.Leu1871=) c.1937G>T c.2124G>T (p.Leu708=) c.*5333G>T (n.*5333G>T) c.*64G>T (n.*64G>T) c.480G>T (p.Leu160=) c.1023G>T (p.Leu341=) c.249G>T (p.Leu83=) n.5686G>T n.5727G>T | ClinVar dbSNP |
17 | g.43045720C= | CA2260761053 | BRCA1 | c.5547G= (p.Leu1849=) c.5550G= (p.Leu1850=) c.5424G= (p.Leu1808=) c.5544G= (p.Leu1848=) c.5472G= (p.Leu1824=) c.2238G= (p.Leu746=) c.2100G= (p.Leu700=) c.4662G= (p.Leu1554=) c.5427G= (p.Leu1809=) c.5616G= (p.Leu1872=) c.5409G= (p.Leu1803=) c.2112G= (p.Leu704=) n.1433G= n.914G= c.5613G= (p.Leu1871=) c.1937G= c.2124G= (p.Leu708=) c.*5333G= (n.*5333G=) c.*64G= (n.*64G=) c.480G= (p.Leu160=) c.1023G= (p.Leu341=) c.249G= (p.Leu83=) n.5686G= n.5727G= | |
17 | g.43045720C>G | CA003709 | BRCA1 | c.5547G>C (p.Leu1849=) c.5550G>C (p.Leu1850=) c.5424G>C (p.Leu1808=) c.5544G>C (p.Leu1848=) c.5472G>C (p.Leu1824=) c.2238G>C (p.Leu746=) c.2100G>C (p.Leu700=) c.4662G>C (p.Leu1554=) c.5427G>C (p.Leu1809=) c.5616G>C (p.Leu1872=) c.5409G>C (p.Leu1803=) c.2112G>C (p.Leu704=) n.1433G>C n.914G>C c.5613G>C (p.Leu1871=) c.1937G>C c.2124G>C (p.Leu708=) c.*5333G>C (n.*5333G>C) c.*64G>C (n.*64G>C) c.480G>C (p.Leu160=) c.1023G>C (p.Leu341=) c.249G>C (p.Leu83=) n.5686G>C n.5727G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.43045720C>T | CA16609840 | BRCA1 | c.5547G>A (p.Leu1849=) c.5550G>A (p.Leu1850=) c.5424G>A (p.Leu1808=) c.5544G>A (p.Leu1848=) c.5472G>A (p.Leu1824=) c.2238G>A (p.Leu746=) c.2100G>A (p.Leu700=) c.4662G>A (p.Leu1554=) c.5427G>A (p.Leu1809=) c.5616G>A (p.Leu1872=) c.5409G>A (p.Leu1803=) c.2112G>A (p.Leu704=) n.1433G>A n.914G>A c.5613G>A (p.Leu1871=) c.1937G>A c.2124G>A (p.Leu708=) c.*5333G>A (n.*5333G>A) c.*64G>A (n.*64G>A) c.480G>A (p.Leu160=) c.1023G>A (p.Leu341=) c.249G>A (p.Leu83=) n.5686G>A n.5727G>A | ClinVar dbSNP |
17 | g.43045721A= | CA2260761055 | BRCA1 | c.5546T= (p.Leu1849=) c.5549T= (p.Leu1850=) c.5423T= (p.Leu1808=) c.5543T= (p.Leu1848=) c.5471T= (p.Leu1824=) c.2237T= (p.Leu746=) c.2099T= (p.Leu700=) c.4661T= (p.Leu1554=) c.5426T= (p.Leu1809=) c.5615T= (p.Leu1872=) c.5408T= (p.Leu1803=) c.2111T= (p.Leu704=) n.1432T= n.913T= c.5612T= (p.Leu1871=) c.1936T= c.2123T= (p.Leu708=) c.*5332T= (n.*5332T=) c.*63T= (n.*63T=) c.479T= (p.Leu160=) c.1022T= (p.Leu341=) c.248T= (p.Leu83=) n.5685T= n.5726T= | |
17 | g.43045721A>C | CA10590221 | BRCA1 | c.5546T>G (p.Leu1849Arg) c.5549T>G (p.Leu1850Arg) c.5423T>G (p.Leu1808Arg) c.5543T>G (p.Leu1848Arg) c.5471T>G (p.Leu1824Arg) c.2237T>G (p.Leu746Arg) c.2099T>G (p.Leu700Arg) c.4661T>G (p.Leu1554Arg) c.5426T>G (p.Leu1809Arg) c.5615T>G (p.Leu1872Arg) c.5408T>G (p.Leu1803Arg) c.2111T>G (p.Leu704Arg) n.1432T>G n.913T>G c.5612T>G (p.Leu1871Arg) c.1936T>G c.2123T>G (p.Leu708Arg) c.*5332T>G (n.*5332T>G) c.*63T>G (n.*63T>G) c.479T>G (p.Leu160Arg) c.1022T>G (p.Leu341Arg) c.248T>G (p.Leu83Arg) n.5685T>G n.5726T>G | ClinVar dbSNP |
17 | g.43045721A>G | CA10590222 | BRCA1 | c.5546T>C (p.Leu1849Pro) c.5549T>C (p.Leu1850Pro) c.5423T>C (p.Leu1808Pro) c.5543T>C (p.Leu1848Pro) c.5471T>C (p.Leu1824Pro) c.2237T>C (p.Leu746Pro) c.2099T>C (p.Leu700Pro) c.4661T>C (p.Leu1554Pro) c.5426T>C (p.Leu1809Pro) c.5615T>C (p.Leu1872Pro) c.5408T>C (p.Leu1803Pro) c.2111T>C (p.Leu704Pro) n.1432T>C n.913T>C c.5612T>C (p.Leu1871Pro) c.1936T>C c.2123T>C (p.Leu708Pro) c.*5332T>C (n.*5332T>C) c.*63T>C (n.*63T>C) c.479T>C (p.Leu160Pro) c.1022T>C (p.Leu341Pro) c.248T>C (p.Leu83Pro) n.5685T>C n.5726T>C | ClinVar dbSNP |
17 | g.43045721A>T | CA10590223 | BRCA1 | c.5546T>A (p.Leu1849Gln) c.5549T>A (p.Leu1850Gln) c.5423T>A (p.Leu1808Gln) c.5543T>A (p.Leu1848Gln) c.5471T>A (p.Leu1824Gln) c.2237T>A (p.Leu746Gln) c.2099T>A (p.Leu700Gln) c.4661T>A (p.Leu1554Gln) c.5426T>A (p.Leu1809Gln) c.5615T>A (p.Leu1872Gln) c.5408T>A (p.Leu1803Gln) c.2111T>A (p.Leu704Gln) n.1432T>A n.913T>A c.5612T>A (p.Leu1871Gln) c.1936T>A c.2123T>A (p.Leu708Gln) c.*5332T>A (n.*5332T>A) c.*63T>A (n.*63T>A) c.479T>A (p.Leu160Gln) c.1022T>A (p.Leu341Gln) c.248T>A (p.Leu83Gln) n.5685T>A n.5726T>A | ClinVar dbSNP |
17 | g.43045721_43045722delinsAG | CA2260761054 | BRCA1 | c.5545_5546delinsCT (p.Leu1849=) c.5548_5549delinsCT (p.Leu1850=) c.5422_5423delinsCT (p.Leu1808=) c.5542_5543delinsCT (p.Leu1848=) c.5470_5471delinsCT (p.Leu1824=) c.2236_2237delinsCT (p.Leu746=) c.2098_2099delinsCT (p.Leu700=) c.4660_4661delinsCT (p.Leu1554=) c.5425_5426delinsCT (p.Leu1809=) c.5614_5615delinsCT (p.Leu1872=) c.5407_5408delinsCT (p.Leu1803=) c.2110_2111delinsCT (p.Leu704=) n.1431_1432delinsCT n.912_913delinsCT c.5611_5612delinsCT (p.Leu1871=) c.1935_1936delinsCT c.2122_2123delinsCT (p.Leu708=) c.*5331_*5332delinsCT (n.*5331_*5332delinsCT) c.*62_*63delinsCT (n.*62_*63delinsCT) c.478_479delinsCT (p.Leu160=) c.1021_1022delinsCT (p.Leu341=) c.247_248delinsCT (p.Leu83=) n.5684_5685delinsCT n.5725_5726delinsCT | |
17 | g.43045722del | CA003707 | BRCA1 | c.5545del (p.Leu1849TrpfsTer5) c.5548del (p.Leu1850TrpfsTer5) c.5422del (p.Leu1808TrpfsTer5) c.5542del (p.Leu1848TrpfsTer5) c.5470del (p.Leu1824TrpfsTer5) c.2236del (p.Leu746TrpfsTer5) c.2098del (p.Leu700TrpfsTer5) c.4660del (p.Leu1554TrpfsTer5) c.5425del (p.Leu1809TrpfsTer5) c.5614del (p.Leu1872TrpfsTer5) c.5407del (p.Leu1803TrpfsTer5) c.2110del (p.Leu704TrpfsTer5) n.1431del n.912del c.5611del (p.Leu1871TrpfsTer5) c.1935del c.2122del (p.Leu708TrpfsTer5) c.*5331del (n.*5331del) c.*62del (n.*62del) c.478del (p.Leu160TrpfsTer5) c.1021del (p.Leu341TrpfsTer5) c.247del (p.Leu83TrpfsTer5) n.5684del n.5725del | ClinVar dbSNP |
17 | g.43045722G>A | CA500142887 | BRCA1 | c.5545C>T (p.Leu1849=) c.5548C>T (p.Leu1850=) c.5422C>T (p.Leu1808=) c.5542C>T (p.Leu1848=) c.5470C>T (p.Leu1824=) c.2236C>T (p.Leu746=) c.2098C>T (p.Leu700=) c.4660C>T (p.Leu1554=) c.5425C>T (p.Leu1809=) c.5614C>T (p.Leu1872=) c.5407C>T (p.Leu1803=) c.2110C>T (p.Leu704=) n.1431C>T n.912C>T c.5611C>T (p.Leu1871=) c.1935C>T c.2122C>T (p.Leu708=) c.*5331C>T (n.*5331C>T) c.*62C>T (n.*62C>T) c.478C>T (p.Leu160=) c.1021C>T (p.Leu341=) c.247C>T (p.Leu83=) n.5684C>T n.5725C>T | ClinVar dbSNP |
17 | g.43045722G>C | CA10590224 | BRCA1 | c.5545C>G (p.Leu1849Val) c.5548C>G (p.Leu1850Val) c.5422C>G (p.Leu1808Val) c.5542C>G (p.Leu1848Val) c.5470C>G (p.Leu1824Val) c.2236C>G (p.Leu746Val) c.2098C>G (p.Leu700Val) c.4660C>G (p.Leu1554Val) c.5425C>G (p.Leu1809Val) c.5614C>G (p.Leu1872Val) c.5407C>G (p.Leu1803Val) c.2110C>G (p.Leu704Val) n.1431C>G n.912C>G c.5611C>G (p.Leu1871Val) c.1935C>G c.2122C>G (p.Leu708Val) c.*5331C>G (n.*5331C>G) c.*62C>G (n.*62C>G) c.478C>G (p.Leu160Val) c.1021C>G (p.Leu341Val) c.247C>G (p.Leu83Val) n.5684C>G n.5725C>G | ClinVar dbSNP |
17 | g.43045722G= | CA2260761056 | BRCA1 | c.5545C= (p.Leu1849=) c.5548C= (p.Leu1850=) c.5422C= (p.Leu1808=) c.5542C= (p.Leu1848=) c.5470C= (p.Leu1824=) c.2236C= (p.Leu746=) c.2098C= (p.Leu700=) c.4660C= (p.Leu1554=) c.5425C= (p.Leu1809=) c.5614C= (p.Leu1872=) c.5407C= (p.Leu1803=) c.2110C= (p.Leu704=) n.1431C= n.912C= c.5611C= (p.Leu1871=) c.1935C= c.2122C= (p.Leu708=) c.*5331C= (n.*5331C=) c.*62C= (n.*62C=) c.478C= (p.Leu160=) c.1021C= (p.Leu341=) c.247C= (p.Leu83=) n.5684C= n.5725C= | |
17 | g.43045722G>T | CA10590225 | BRCA1 | c.5545C>A (p.Leu1849Met) c.5548C>A (p.Leu1850Met) c.5422C>A (p.Leu1808Met) c.5542C>A (p.Leu1848Met) c.5470C>A (p.Leu1824Met) c.2236C>A (p.Leu746Met) c.2098C>A (p.Leu700Met) c.4660C>A (p.Leu1554Met) c.5425C>A (p.Leu1809Met) c.5614C>A (p.Leu1872Met) c.5407C>A (p.Leu1803Met) c.2110C>A (p.Leu704Met) n.1431C>A n.912C>A c.5611C>A (p.Leu1871Met) c.1935C>A c.2122C>A (p.Leu708Met) c.*5331C>A (n.*5331C>A) c.*62C>A (n.*62C>A) c.478C>A (p.Leu160Met) c.1021C>A (p.Leu341Met) c.247C>A (p.Leu83Met) n.5684C>A n.5725C>A | ClinVar dbSNP |
17 | g.43045723C>A | CA10590226 | BRCA1 | c.5544G>T (p.Glu1848Asp) c.5547G>T (p.Glu1849Asp) c.5421G>T (p.Glu1807Asp) c.5541G>T (p.Glu1847Asp) c.5469G>T (p.Glu1823Asp) c.2235G>T (p.Glu745Asp) c.2097G>T (p.Glu699Asp) c.4659G>T (p.Glu1553Asp) c.5424G>T (p.Glu1808Asp) c.5613G>T (p.Glu1871Asp) c.5406G>T (p.Glu1802Asp) c.2109G>T (p.Glu703Asp) n.1430G>T n.911G>T c.5610G>T (p.Glu1870Asp) c.1934G>T c.2121G>T (p.Glu707Asp) c.*5330G>T (n.*5330G>T) c.*61G>T (n.*61G>T) c.477G>T (p.Glu159Asp) c.1020G>T (p.Glu340Asp) c.246G>T (p.Glu82Asp) n.5683G>T n.5724G>T | ClinVar dbSNP gnomAD v4 |
17 | g.43045723C= | CA2260761057 | BRCA1 | c.5544G= (p.Glu1848=) c.5547G= (p.Glu1849=) c.5421G= (p.Glu1807=) c.5541G= (p.Glu1847=) c.5469G= (p.Glu1823=) c.2235G= (p.Glu745=) c.2097G= (p.Glu699=) c.4659G= (p.Glu1553=) c.5424G= (p.Glu1808=) c.5613G= (p.Glu1871=) c.5406G= (p.Glu1802=) c.2109G= (p.Glu703=) n.1430G= n.911G= c.5610G= (p.Glu1870=) c.1934G= c.2121G= (p.Glu707=) c.*5330G= (n.*5330G=) c.*61G= (n.*61G=) c.477G= (p.Glu159=) c.1020G= (p.Glu340=) c.246G= (p.Glu82=) n.5683G= n.5724G= | |
17 | g.43045723C>G | CA10590227 | BRCA1 | c.5544G>C (p.Glu1848Asp) c.5547G>C (p.Glu1849Asp) c.5421G>C (p.Glu1807Asp) c.5541G>C (p.Glu1847Asp) c.5469G>C (p.Glu1823Asp) c.2235G>C (p.Glu745Asp) c.2097G>C (p.Glu699Asp) c.4659G>C (p.Glu1553Asp) c.5424G>C (p.Glu1808Asp) c.5613G>C (p.Glu1871Asp) c.5406G>C (p.Glu1802Asp) c.2109G>C (p.Glu703Asp) n.1430G>C n.911G>C c.5610G>C (p.Glu1870Asp) c.1934G>C c.2121G>C (p.Glu707Asp) c.*5330G>C (n.*5330G>C) c.*61G>C (n.*61G>C) c.477G>C (p.Glu159Asp) c.1020G>C (p.Glu340Asp) c.246G>C (p.Glu82Asp) n.5683G>C n.5724G>C | ClinVar dbSNP |
17 | g.43045723C>T | CA500142888 | BRCA1 | c.5544G>A (p.Glu1848=) c.5547G>A (p.Glu1849=) c.5421G>A (p.Glu1807=) c.5541G>A (p.Glu1847=) c.5469G>A (p.Glu1823=) c.2235G>A (p.Glu745=) c.2097G>A (p.Glu699=) c.4659G>A (p.Glu1553=) c.5424G>A (p.Glu1808=) c.5613G>A (p.Glu1871=) c.5406G>A (p.Glu1802=) c.2109G>A (p.Glu703=) n.1430G>A n.911G>A c.5610G>A (p.Glu1870=) c.1934G>A c.2121G>A (p.Glu707=) c.*5330G>A (n.*5330G>A) c.*61G>A (n.*61G>A) c.477G>A (p.Glu159=) c.1020G>A (p.Glu340=) c.246G>A (p.Glu82=) n.5683G>A n.5724G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.43045724T>A | CA10590228 | BRCA1 | c.5543A>T (p.Glu1848Val) c.5546A>T (p.Glu1849Val) c.5420A>T (p.Glu1807Val) c.5540A>T (p.Glu1847Val) c.5468A>T (p.Glu1823Val) c.2234A>T (p.Glu745Val) c.2096A>T (p.Glu699Val) c.4658A>T (p.Glu1553Val) c.5423A>T (p.Glu1808Val) c.5612A>T (p.Glu1871Val) c.5405A>T (p.Glu1802Val) c.2108A>T (p.Glu703Val) n.1429A>T n.910A>T c.5609A>T (p.Glu1870Val) c.1933A>T c.2120A>T (p.Glu707Val) c.*5329A>T (n.*5329A>T) c.*60A>T (n.*60A>T) c.476A>T (p.Glu159Val) c.1019A>T (p.Glu340Val) c.245A>T (p.Glu82Val) n.5682A>T n.5723A>T | ClinVar dbSNP |
17 | g.43045724T>C | CA10590229 | BRCA1 | c.5543A>G (p.Glu1848Gly) c.5546A>G (p.Glu1849Gly) c.5420A>G (p.Glu1807Gly) c.5540A>G (p.Glu1847Gly) c.5468A>G (p.Glu1823Gly) c.2234A>G (p.Glu745Gly) c.2096A>G (p.Glu699Gly) c.4658A>G (p.Glu1553Gly) c.5423A>G (p.Glu1808Gly) c.5612A>G (p.Glu1871Gly) c.5405A>G (p.Glu1802Gly) c.2108A>G (p.Glu703Gly) n.1429A>G n.910A>G c.5609A>G (p.Glu1870Gly) c.1933A>G c.2120A>G (p.Glu707Gly) c.*5329A>G (n.*5329A>G) c.*60A>G (n.*60A>G) c.476A>G (p.Glu159Gly) c.1019A>G (p.Glu340Gly) c.245A>G (p.Glu82Gly) n.5682A>G n.5723A>G | ClinVar dbSNP |
17 | g.43045724T>G | CA10590230 | BRCA1 | c.5543A>C (p.Glu1848Ala) c.5546A>C (p.Glu1849Ala) c.5420A>C (p.Glu1807Ala) c.5540A>C (p.Glu1847Ala) c.5468A>C (p.Glu1823Ala) c.2234A>C (p.Glu745Ala) c.2096A>C (p.Glu699Ala) c.4658A>C (p.Glu1553Ala) c.5423A>C (p.Glu1808Ala) c.5612A>C (p.Glu1871Ala) c.5405A>C (p.Glu1802Ala) c.2108A>C (p.Glu703Ala) n.1429A>C n.910A>C c.5609A>C (p.Glu1870Ala) c.1933A>C c.2120A>C (p.Glu707Ala) c.*5329A>C (n.*5329A>C) c.*60A>C (n.*60A>C) c.476A>C (p.Glu159Ala) c.1019A>C (p.Glu340Ala) c.245A>C (p.Glu82Ala) n.5682A>C n.5723A>C | ClinVar dbSNP |
17 | g.43045724T= | CA2260761059 | BRCA1 | c.5543A= (p.Glu1848=) c.5546A= (p.Glu1849=) c.5420A= (p.Glu1807=) c.5540A= (p.Glu1847=) c.5468A= (p.Glu1823=) c.2234A= (p.Glu745=) c.2096A= (p.Glu699=) c.4658A= (p.Glu1553=) c.5423A= (p.Glu1808=) c.5612A= (p.Glu1871=) c.5405A= (p.Glu1802=) c.2108A= (p.Glu703=) n.1429A= n.910A= c.5609A= (p.Glu1870=) c.1933A= c.2120A= (p.Glu707=) c.*5329A= (n.*5329A=) c.*60A= (n.*60A=) c.476A= (p.Glu159=) c.1019A= (p.Glu340=) c.245A= (p.Glu82=) n.5682A= n.5723A= | |
17 | g.43045724_43045727delinsTCCT | CA2260761058 | BRCA1 | c.5540_5543delinsAGGA (p.Gln1847=) c.5543_5546delinsAGGA (p.Gln1848=) c.5417_5420delinsAGGA (p.Gln1806=) c.5537_5540delinsAGGA (p.Gln1846=) c.5465_5468delinsAGGA (p.Gln1822=) c.2231_2234delinsAGGA (p.Gln744=) c.2093_2096delinsAGGA (p.Gln698=) c.4655_4658delinsAGGA (p.Gln1552=) c.5420_5423delinsAGGA (p.Gln1807=) c.5609_5612delinsAGGA (p.Gln1870=) c.5402_5405delinsAGGA (p.Gln1801=) c.2105_2108delinsAGGA (p.Gln702=) n.1426_1429delinsAGGA n.907_910delinsAGGA c.5606_5609delinsAGGA (p.Gln1869=) c.1930_1933delinsAGGA c.2117_2120delinsAGGA (p.Gln706=) c.*5326_*5329delinsAGGA (n.*5326_*5329delinsAGGA) c.*57_*60delinsAGGA (n.*57_*60delinsAGGA) c.473_476delinsAGGA (p.Gln158=) c.1016_1019delinsAGGA (p.Gln339=) c.242_245delinsAGGA (p.Gln81=) n.5679_5682delinsAGGA n.5720_5723delinsAGGA | |
17 | g.43045725C>A | CA10590231 | BRCA1 | c.5542G>T (p.Glu1848Ter) c.5545G>T (p.Glu1849Ter) c.5419G>T (p.Glu1807Ter) c.5539G>T (p.Glu1847Ter) c.5467G>T (p.Glu1823Ter) c.2233G>T (p.Glu745Ter) c.2095G>T (p.Glu699Ter) c.4657G>T (p.Glu1553Ter) c.5422G>T (p.Glu1808Ter) c.5611G>T (p.Glu1871Ter) c.5404G>T (p.Glu1802Ter) c.2107G>T (p.Glu703Ter) n.1428G>T n.909G>T c.5608G>T (p.Glu1870Ter) c.1932G>T c.2119G>T (p.Glu707Ter) c.*5328G>T (n.*5328G>T) c.*59G>T (n.*59G>T) c.475G>T (p.Glu159Ter) c.1018G>T (p.Glu340Ter) c.244G>T (p.Glu82Ter) n.5681G>T n.5722G>T | ClinVar dbSNP |