ClinVar Miner

List of variants in gene BRAF reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 25
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HGVS dbSNP
NM_004333.4(BRAF):c.*7T>C rs727502903
NM_004333.4(BRAF):c.-19C>T rs71645935
NM_004333.4(BRAF):c.1084C>A (p.Arg362=) rs397516885
NM_004333.4(BRAF):c.1203C>T (p.Thr401=) rs370130654
NM_004333.4(BRAF):c.1209T>C (p.Pro403=) rs397516887
NM_004333.4(BRAF):c.1347T>C (p.Asp449=) rs397516889
NM_004333.4(BRAF):c.1960T>C (p.Leu654=) rs727502905
NM_004333.4(BRAF):c.2128-10T>C rs397516898
NM_004333.4(BRAF):c.2128-5delT rs373442098
NM_004333.4(BRAF):c.2136C>T (p.Ala712=) rs377165711
NM_004333.4(BRAF):c.2229T>C (p.Phe743=) rs397516901
NM_004333.5(BRAF):c.1068A>G (p.Gln356=) rs143335467
NM_004333.5(BRAF):c.111G>A (p.Ser37=) rs727502906
NM_004333.5(BRAF):c.1236C>T (p.Asn412=) rs397516888
NM_004333.5(BRAF):c.1632T>C (p.Ile544=) rs149702741
NM_004333.5(BRAF):c.1694+14G>A rs184144181
NM_004333.5(BRAF):c.1993-11dup rs759069424
NM_004333.5(BRAF):c.2128-6T>A rs397516900
NM_004333.5(BRAF):c.375T>G (p.Ser125=) rs201507202
NM_004333.5(BRAF):c.483G>C (p.Leu161=) rs61730029
NM_004333.5(BRAF):c.622A>G (p.Ile208Val) rs727504571
NM_004333.5(BRAF):c.708C>T (p.Asn236=) rs138333692
NM_004333.5(BRAF):c.714A>T (p.Val238=) rs397516902
NM_004333.5(BRAF):c.92C>G (p.Ala31Gly) rs397516906
NM_004333.5(BRAF):c.95_100del (p.Gly32_Ala33del) rs397507458

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