ClinVar Miner

List of variants in gene BRAF reported as uncertain significance for cancer

Included ClinVar conditions (475):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 139
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HGVS dbSNP gnomAD frequency
NM_004333.6(BRAF):c.1180T>C (p.Ser394Pro) rs923739321 0.00004
NM_004333.6(BRAF):c.2140A>G (p.Ile714Val) rs555976452 0.00003
NM_004333.6(BRAF):c.112G>C (p.Ala38Pro) rs1011563467 0.00001
NM_004333.6(BRAF):c.1166G>A (p.Arg389His) rs577372072 0.00001
NM_004333.6(BRAF):c.1237G>A (p.Val413Met) rs377093637 0.00001
NM_004333.6(BRAF):c.26G>C (p.Gly9Ala) rs1211436028 0.00001
NM_004333.6(BRAF):c.437G>A (p.Arg146Gln) rs557241012 0.00001
NM_004333.6(BRAF):c.1205C>A (p.Pro402His) rs199927105
NM_004333.6(BRAF):c.124G>T (p.Ala42Ser) rs2129153151
NM_004333.6(BRAF):c.1315-15A>T
NM_004333.6(BRAF):c.1315-35T>A
NM_004333.6(BRAF):c.1321C>T (p.Leu441Phe)
NM_004333.6(BRAF):c.1323T>G (p.Leu441=)
NM_004333.6(BRAF):c.1326T>G (p.Gly442=)
NM_004333.6(BRAF):c.1333G>T (p.Asp445Tyr)
NM_004333.6(BRAF):c.1335C>T (p.Asp445=)
NM_004333.6(BRAF):c.1337C>A (p.Ser446Ter)
NM_004333.6(BRAF):c.1338G>T (p.Ser446=)
NM_004333.6(BRAF):c.1339A>T (p.Ser447Cys)
NM_004333.6(BRAF):c.1342_1343insT (p.Asp448fs)
NM_004333.6(BRAF):c.1348_1349insC (p.Trp450fs)
NM_004333.6(BRAF):c.1351dup (p.Glu451fs)
NM_004333.6(BRAF):c.1353_1354insC (p.Ile452fs)
NM_004333.6(BRAF):c.1358C>T (p.Pro453Leu)
NM_004333.6(BRAF):c.1365del (p.Gln456fs)
NM_004333.6(BRAF):c.1367A>T (p.Gln456Leu)
NM_004333.6(BRAF):c.1368dup (p.Ile457fs)
NM_004333.6(BRAF):c.1371del (p.Thr458fs)
NM_004333.6(BRAF):c.1372A>C (p.Thr458Pro)
NM_004333.6(BRAF):c.1373del (p.Thr458fs)
NM_004333.6(BRAF):c.1375_1376insC (p.Val459fs)
NM_004333.6(BRAF):c.1375dup (p.Val459fs)
NM_004333.6(BRAF):c.1376T>G (p.Val459Gly)
NM_004333.6(BRAF):c.1377_1378insT (p.Gly460fs)
NM_004333.6(BRAF):c.1379G>A (p.Gly460Glu)
NM_004333.6(BRAF):c.1379del (p.Gly460fs)
NM_004333.6(BRAF):c.1388T>C (p.Ile463Thr)
NM_004333.6(BRAF):c.1389T>C (p.Ile463=)
NM_004333.6(BRAF):c.1390G>A (p.Gly464Arg) rs121913349
NM_004333.6(BRAF):c.1395del (p.Gly466fs)
NM_004333.6(BRAF):c.1404T>G (p.Phe468Leu)
NM_004333.6(BRAF):c.1404_1405del (p.Phe468fs)
NM_004333.6(BRAF):c.1408A>G (p.Thr470Ala)
NM_004333.6(BRAF):c.1413C>T (p.Val471=)
NM_004333.6(BRAF):c.1415A>C (p.Tyr472Ser)
NM_004333.6(BRAF):c.1415A>G (p.Tyr472Cys) rs1057519719
NM_004333.6(BRAF):c.1416_1417insT (p.Lys473Ter)
NM_004333.6(BRAF):c.1426T>G (p.Trp476Gly)
NM_004333.6(BRAF):c.1428_1429insA (p.His477fs)
NM_004333.6(BRAF):c.1430A>C (p.His477Pro)
NM_004333.6(BRAF):c.1432+102C>A
NM_004333.6(BRAF):c.1432+114A>G
NM_004333.6(BRAF):c.1432+120A>T
NM_004333.6(BRAF):c.1432+128C>T
NM_004333.6(BRAF):c.1432+136C>T
NM_004333.6(BRAF):c.1432+141A>C
NM_004333.6(BRAF):c.1432+142A>C
NM_004333.6(BRAF):c.1432+144G>A
NM_004333.6(BRAF):c.1432+157A>G
NM_004333.6(BRAF):c.1432+15T>A
NM_004333.6(BRAF):c.1432+176G>C
NM_004333.6(BRAF):c.1432+181C>T
NM_004333.6(BRAF):c.1432+18del
NM_004333.6(BRAF):c.1432+201A>T
NM_004333.6(BRAF):c.1432+20A>C
NM_004333.6(BRAF):c.1432+20A>G
NM_004333.6(BRAF):c.1432+20A>T
NM_004333.6(BRAF):c.1432+22A>T
NM_004333.6(BRAF):c.1432+230G>A
NM_004333.6(BRAF):c.1432+234T>A
NM_004333.6(BRAF):c.1432+237T>C
NM_004333.6(BRAF):c.1432+246A>G
NM_004333.6(BRAF):c.1432+276T>G
NM_004333.6(BRAF):c.1432+282C>T
NM_004333.6(BRAF):c.1432+296T>A
NM_004333.6(BRAF):c.1432+296T>C
NM_004333.6(BRAF):c.1432+298T>G
NM_004333.6(BRAF):c.1432+304G>T
NM_004333.6(BRAF):c.1432+306A>G
NM_004333.6(BRAF):c.1432+308T>A
NM_004333.6(BRAF):c.1432+33T>C
NM_004333.6(BRAF):c.1432+34C>G
NM_004333.6(BRAF):c.1432+34C>T
NM_004333.6(BRAF):c.1432+35A>G
NM_004333.6(BRAF):c.1432+38A>C
NM_004333.6(BRAF):c.1432+3A>T
NM_004333.6(BRAF):c.1432+41G>A
NM_004333.6(BRAF):c.1432+43A>T
NM_004333.6(BRAF):c.1432+46T>C
NM_004333.6(BRAF):c.1432+52A>T
NM_004333.6(BRAF):c.1432+65T>G
NM_004333.6(BRAF):c.1432+67T>C
NM_004333.6(BRAF):c.1432+8T>C
NM_004333.6(BRAF):c.1432+95C>T
NM_004333.6(BRAF):c.1695-10145T>A
NM_004333.6(BRAF):c.1695-10150C>T
NM_004333.6(BRAF):c.1695-10155T>A
NM_004333.6(BRAF):c.1695-10157C>G
NM_004333.6(BRAF):c.1695-10193A>T
NM_004333.6(BRAF):c.1695-10204C>T
NM_004333.6(BRAF):c.1695-10229T>A
NM_004333.6(BRAF):c.1695-10233C>T
NM_004333.6(BRAF):c.1695-10273A>G
NM_004333.6(BRAF):c.1695-10278G>A
NM_004333.6(BRAF):c.1695-10286G>T
NM_004333.6(BRAF):c.1695-10293G>A
NM_004333.6(BRAF):c.1695-10295A>G
NM_004333.6(BRAF):c.1695-10306G>A
NM_004333.6(BRAF):c.1695-10335A>G
NM_004333.6(BRAF):c.1695-10342T>A
NM_004333.6(BRAF):c.1695-10345G>T
NM_004333.6(BRAF):c.1695-10356G>A
NM_004333.6(BRAF):c.1695-10377G>A
NM_004333.6(BRAF):c.1695-10389T>C
NM_004333.6(BRAF):c.1695-10396G>T
NM_004333.6(BRAF):c.1695-10408A>G
NM_004333.6(BRAF):c.1695-10455A>G
NM_004333.6(BRAF):c.1695-10462T>G
NM_004333.6(BRAF):c.1695-10468C>T
NM_004333.6(BRAF):c.1695-10472del
NM_004333.6(BRAF):c.1742-10T>A
NM_004333.6(BRAF):c.1742-13T>G
NM_004333.6(BRAF):c.1742-15C>A
NM_004333.6(BRAF):c.1742-16del
NM_004333.6(BRAF):c.1742-1delinsTT
NM_004333.6(BRAF):c.1759G>A (p.Asp587Asn) rs2128998452
NM_004333.6(BRAF):c.1768dup (p.Val590fs)
NM_004333.6(BRAF):c.1769_1770insTTAGA (p.Val590_Lys591insTer)
NM_004333.6(BRAF):c.1771A>G (p.Lys591Glu)
NM_004333.6(BRAF):c.1776A>T (p.Ile592=)
NM_004333.6(BRAF):c.1778_1779insATG (p.Gly593_Asp594insCys)
NM_004333.6(BRAF):c.1780G>A (p.Asp594Asn) rs397516896
NM_004333.6(BRAF):c.1782_1783insATT (p.Asp594_Phe595insIle)
NM_004333.6(BRAF):c.1783T>C (p.Phe595Leu) rs794729219
NM_004333.6(BRAF):c.1860+21del
NM_004333.6(BRAF):c.1860+38del
NM_004333.6(BRAF):c.1897T>C (p.Tyr633His) rs746010267
NM_004333.6(BRAF):c.1940A>G (p.Tyr647Cys) rs1562939198
NM_004333.6(BRAF):c.260G>A (p.Ser87Asn) rs1033856250

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