ClinVar Miner

List of variants in gene BRAF reported as benign by Integrated Genetics/Laboratory Corporation of America

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_001374258.1(BRAF):c.-19C>T rs71645935
NM_001374258.1(BRAF):c.1068A>G (p.Gln356=) rs143335467
NM_001374258.1(BRAF):c.1452G>A (p.Arg484=) rs56101602
NM_001374258.1(BRAF):c.1553-19A>G rs369635503
NM_001374258.1(BRAF):c.1814+14G>A rs184144181
NM_001374258.1(BRAF):c.2049A>G (p.Gly683=) rs9648696
NM_001374258.1(BRAF):c.2112+16G>C rs3789806
NM_001374258.1(BRAF):c.2247+3A>G rs371976102
NM_001374258.1(BRAF):c.2248-16_2248-7del
NM_001374258.1(BRAF):c.2248-16del
NM_001374258.1(BRAF):c.2248-26dup
NM_001374258.1(BRAF):c.2248-27_2248-18del
NM_001374258.1(BRAF):c.375T>G (p.Ser125=) rs201507202
NM_001374258.1(BRAF):c.483G>C (p.Leu161=) rs61730029
NM_001374258.1(BRAF):c.64G>A (p.Asp22Asn) rs397507456
NM_001374258.1(BRAF):c.708C>T (p.Asn236=) rs138333692
NM_004333.6(BRAF):c.-5A>G rs71645936
NM_004333.6(BRAF):c.1141-19C>T rs71645959
NM_004333.6(BRAF):c.1150A>G (p.Arg384Gly) rs545495379
NM_004333.6(BRAF):c.1315-18T>G rs6959000
NM_004333.6(BRAF):c.138+17C>G rs756400234
NM_004333.6(BRAF):c.1517+20T>C rs71645980
NM_004333.6(BRAF):c.1992+16G>A rs3789806
NM_004333.6(BRAF):c.2128-15dup rs373442098
NM_004333.6(BRAF):c.2128-16C>T rs368721021
NM_004333.6(BRAF):c.2136C>T (p.Ala712=) rs377165711
NM_004333.6(BRAF):c.36G>A (p.Ala12=) rs397507454
NM_004333.6(BRAF):c.399A>G (p.Ser133=) rs397507463
NM_004333.6(BRAF):c.608+19G>C rs200908826
NM_004333.6(BRAF):c.68T>A (p.Met23Lys) rs746778122
NM_004333.6(BRAF):c.951C>A (p.Ser317=) rs755298519
NM_004333.6(BRAF):c.976A>G (p.Ile326Val) rs775040765

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