ClinVar Miner

List of variants in gene MSH6 reported as uncertain significance by Biesecker Lab/Human Development Section,National Institutes of Health

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Total variants: 12
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HGVS dbSNP
NM_000179.2(MSH6):c.1099C>A (p.His367Asn) rs201193496
NM_000179.2(MSH6):c.1186C>G (p.Leu396Val) rs2020908
NM_000179.2(MSH6):c.1390A>T (p.Ile464Phe) rs201892477
NM_000179.2(MSH6):c.1526T>C (p.Val509Ala) rs63751005
NM_000179.2(MSH6):c.1618C>A (p.Leu540Ile) rs201996928
NM_000179.2(MSH6):c.1867C>G (p.Pro623Ala) rs3136334
NM_000179.2(MSH6):c.2667G>T (p.Gln889His) rs149945495
NM_000179.2(MSH6):c.3038A>C (p.Lys1013Thr) rs200837944
NM_000179.2(MSH6):c.3217C>T (p.Pro1073Ser) rs142254875
NM_000179.2(MSH6):c.3833C>G (p.Pro1278Arg) rs201191389
NM_000179.2(MSH6):c.4071_4074dup (p.Glu1359Ter) rs386833407
NM_000179.2(MSH6):c.431G>T (p.Ser144Ile) rs3211299

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