ClinVar Miner

List of variants in gene MSH6 reported as likely benign for breast cancer

Included ClinVar conditions (61):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_000179.3(MSH6):c.984C>T (p.Ser328=) rs138143769 0.00101
NM_000179.3(MSH6):c.1449G>T (p.Val483=) rs35590297 0.00037
NM_000179.3(MSH6):c.3160A>T (p.Ile1054Phe) rs267608075 0.00016
NM_000179.3(MSH6):c.3203G>A (p.Arg1068Gln) rs398123230 0.00012
NM_000179.3(MSH6):c.1050C>T (p.Ala350=) rs730881802 0.00006
NM_000179.3(MSH6):c.3282A>T (p.Ser1094=) rs372996269 0.00006
NM_000179.3(MSH6):c.3625C>T (p.Leu1209=) rs753675331 0.00001
NM_000179.3(MSH6):c.3879T>C (p.Ala1293=) rs752369374 0.00001
NM_000179.3(MSH6):c.417A>G (p.Thr139=) rs758390144 0.00001
NM_000179.3(MSH6):c.1233G>A (p.Arg411=) rs554843104
NM_000179.3(MSH6):c.24C>T (p.Tyr8=) rs746306598
NM_000179.3(MSH6):c.3162C>T (p.Ile1054=) rs149605979
NM_000179.3(MSH6):c.3647-6T>C rs182871847
NM_000179.3(MSH6):c.4001+2TAAC[2] rs267608132
NM_000179.3(MSH6):c.4001+2TAAC[4] rs267608132
NM_000179.3(MSH6):c.597C>T (p.Pro199=) rs1553411498
NM_000179.3(MSH6):c.628-13C>G rs538280815
NM_000179.3(MSH6):c.957G>A (p.Thr319=) rs375210430

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