ClinVar Miner

List of variants in gene BRAF reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_004333.6(BRAF):c.1141-110G>A rs117001169 0.00440
NM_004333.6(BRAF):c.1177+1073C>T rs147309367 0.00385
NM_004333.6(BRAF):c.1227A>G (p.Ser409=) rs145035762 0.00318
NM_004333.6(BRAF):c.1178-271T>C rs189649654 0.00292
NM_004333.6(BRAF):c.1140+2523G>C rs190814468 0.00278
NM_004333.6(BRAF):c.1177+959A>G rs189896094 0.00124
NM_004333.6(BRAF):c.1332G>A (p.Arg444=) rs56101602 0.00068
NM_004333.6(BRAF):c.980+1812C>T rs1046366661 0.00030
NM_004333.6(BRAF):c.64G>A (p.Asp22Asn) rs397507456 0.00025
NM_004333.6(BRAF):c.723G>A (p.Thr241=) rs369182143 0.00013
NM_004333.6(BRAF):c.36G>A (p.Ala12=) rs397507454 0.00011
NM_004333.6(BRAF):c.375T>G (p.Ser125=) rs201507202 0.00008
NM_004333.6(BRAF):c.2196C>G (p.Ser732=) rs142592480 0.00005
NM_004333.6(BRAF):c.72G>C (p.Glu24Asp) rs587778114 0.00005
NM_004333.6(BRAF):c.708C>T (p.Asn236=) rs138333692 0.00003
NM_004333.6(BRAF):c.240+6C>T rs1320075163 0.00002
NM_004333.6(BRAF):c.357C>T (p.Thr119=) rs552456345 0.00002
NM_004333.6(BRAF):c.1347T>C (p.Asp449=) rs397516889 0.00001
NM_004333.6(BRAF):c.1818G>A (p.Gly606=) rs1797931923 0.00001
NM_004333.6(BRAF):c.951C>A (p.Ser317=) rs755298519 0.00001
NC_000007.14:g.140798273_140798276T[4]CTTTTTTTTTTT[1]
NC_000007.14:g.140798273_140798279T[7]CTTTTTTTTTTT[1]
NM_001374258.1(BRAF):c.*124C>T
NM_004333.6(BRAF):c.1140+1204T>C
NM_004333.6(BRAF):c.1140+2154G>T
NM_004333.6(BRAF):c.1140+2157A>G
NM_004333.6(BRAF):c.1140+2236T>C
NM_004333.6(BRAF):c.1140+2553_1140+2554del
NM_004333.6(BRAF):c.1140+2738G>A
NM_004333.6(BRAF):c.1140+3283G>A
NM_004333.6(BRAF):c.1140+3314C>T
NM_004333.6(BRAF):c.1140+804_1140+805insTA
NM_004333.6(BRAF):c.1140+815A>G
NM_004333.6(BRAF):c.1141-1355C>T
NM_004333.6(BRAF):c.1141-137T>C
NM_004333.6(BRAF):c.1141-1927C>T
NM_004333.6(BRAF):c.1141-1946G>A
NM_004333.6(BRAF):c.1141-2272C>T
NM_004333.6(BRAF):c.1141-3287G>A
NM_004333.6(BRAF):c.1141-370C>T
NM_004333.6(BRAF):c.1141-529G>T
NM_004333.6(BRAF):c.1141-563A>T
NM_004333.6(BRAF):c.1141-58C>T
NM_004333.6(BRAF):c.1141-632A>G
NM_004333.6(BRAF):c.1177+1386G>A
NM_004333.6(BRAF):c.1177+1621C>T
NM_004333.6(BRAF):c.1177+2114C>T
NM_004333.6(BRAF):c.1177+2192T>G
NM_004333.6(BRAF):c.1177+245_1177+247dup rs1199383417
NM_004333.6(BRAF):c.1178-1093G>T
NM_004333.6(BRAF):c.1178-1184C>T
NM_004333.6(BRAF):c.1178-1954dup
NM_004333.6(BRAF):c.1178-860T>G
NM_004333.6(BRAF):c.1178-946_1178-943dup
NM_004333.6(BRAF):c.1206C>A (p.Pro402=) rs201758035
NM_004333.6(BRAF):c.1315-105C>G
NM_004333.6(BRAF):c.1315-131T>C
NM_004333.6(BRAF):c.1315-407A>G
NM_004333.6(BRAF):c.141G>A (p.Val47=) rs2129073776
NM_004333.6(BRAF):c.2128-16_2128-7del rs766844227
NM_004333.6(BRAF):c.2128-27_2128-18del rs774138098
NM_004333.6(BRAF):c.288A>G (p.Glu96=)
NM_004333.6(BRAF):c.342T>C (p.Ser114=)
NM_004333.6(BRAF):c.406T>G (p.Ser136Ala)
NM_004333.6(BRAF):c.738A>G (p.Ala246=) rs1586213511
NM_004333.6(BRAF):c.83GCGCCG[2] (p.28GA[2]) rs397507458
NM_004333.6(BRAF):c.980+1221G>A
NM_004333.6(BRAF):c.980+1615C>T
NM_004333.6(BRAF):c.980+1809del
NM_004333.6(BRAF):c.980+2064A>G
NM_004333.6(BRAF):c.980+2510T>A
NM_004333.6(BRAF):c.980+2726G>T
NM_004333.6(BRAF):c.980+2809G>A
NM_004333.6(BRAF):c.980+483C>A
NM_004333.6(BRAF):c.980+601T>C
NM_004333.6(BRAF):c.980+812T>C
NM_004333.6(BRAF):c.981-1264A>G
NM_004333.6(BRAF):c.981-1315dup
NM_004333.6(BRAF):c.981-2805G>C
NM_004333.6(BRAF):c.981-2908A>G

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