ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_004333.6(BRAF):c.78G>T (p.Glu26Asp) rs371877084 0.01088
NM_004333.6(BRAF):c.1314+475C>T rs186563964 0.01004
NM_004333.6(BRAF):c.1178-1573G>A rs193184404 0.00414
NM_004333.6(BRAF):c.1383A>G (p.Gln461=) rs56216404 0.00399
NM_004333.6(BRAF):c.1141-1276T>C rs183532604 0.00259
NM_004333.6(BRAF):c.1141-497A>G rs186712243 0.00234
NM_004333.6(BRAF):c.980+2878C>G rs577616802 0.00233
NM_004333.6(BRAF):c.2235A>G (p.Leu745=) rs56046546 0.00030
NM_004333.6(BRAF):c.981-2232A>T rs183923001 0.00021
NM_004333.6(BRAF):c.504+17A>G rs201797624 0.00013
NM_004333.6(BRAF):c.1140+1346A>G
NM_004333.6(BRAF):c.1140+2410A>G
NM_004333.6(BRAF):c.1140+3107C>T
NM_004333.6(BRAF):c.1140+648G>C
NM_004333.6(BRAF):c.1141-1346C>T
NM_004333.6(BRAF):c.1141-1792A>G
NM_004333.6(BRAF):c.1141-2047A>G
NM_004333.6(BRAF):c.1141-2721A>G
NM_004333.6(BRAF):c.1141-465C>T
NM_004333.6(BRAF):c.1177+1932C>T
NM_004333.6(BRAF):c.1178-1374C>G
NM_004333.6(BRAF):c.1178-1791C>T
NM_004333.6(BRAF):c.1178-896A>G
NM_004333.6(BRAF):c.1315-305C>T
NM_004333.6(BRAF):c.1315-388G>T
NM_004333.6(BRAF):c.138+80G>A
NM_004333.6(BRAF):c.980+1670G>A
NM_004333.6(BRAF):c.980+2099del
NM_004333.6(BRAF):c.980+2523T>A
NM_004333.6(BRAF):c.981-1309A>G
NM_004333.6(BRAF):c.981-811C>T
NM_004333.6(BRAF):c.981-967A>G

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