ClinVar Miner

List of variants in gene MSH6 reported as pathogenic by Counsyl

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Total variants: 17
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HGVS dbSNP
NM_000179.2 (MSH6):c.3984_3987dupGTCA (p.Leu1330Valfs) rs267608121
NM_000179.2(MSH6):c.10C>T (p.Gln4Ter) rs786201042
NM_000179.2(MSH6):c.1346T>C (p.Leu449Pro) rs63750741
NM_000179.2(MSH6):c.1350_1351delAT (p.Phe451Hisfs) rs878853702
NM_000179.2(MSH6):c.1444C>T (p.Arg482Ter) rs63750909
NM_000179.2(MSH6):c.1805C>G (p.Ser602Ter) rs730881816
NM_000179.2(MSH6):c.2150_2153delTCAG (p.Val717Alafs) rs267608058
NM_000179.2(MSH6):c.2535dupT (p.Glu846Terfs) rs587779241
NM_000179.2(MSH6):c.2731C>T (p.Arg911Ter) rs63751017
NM_000179.2(MSH6):c.2832_2833delAA (p.Ile944Metfs) rs730881827
NM_000179.2(MSH6):c.3261dupC (p.Phe1088Leufs) rs267608078
NM_000179.2(MSH6):c.3514dupA (p.Arg1172Lysfs) rs63751327
NM_000179.2(MSH6):c.3699_3702delAGAA (p.Lys1233Asnfs) rs193922343
NM_000179.2(MSH6):c.3847_3850dupATTA (p.Thr1284Asnfs) rs267608128
NM_000179.2(MSH6):c.3959_3962delCAAG (p.Ala1320Glufs) rs267608119
NM_000179.2(MSH6):c.3991C>T (p.Arg1331Ter) rs267608094
NM_000179.2(MSH6):c.467C>G (p.Ser156Ter) rs63749873

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