List of variants in gene MSH6 reported as uncertain significance by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.2667G>T (p.Gln889His)	rs149945495	0.00048
NM_000179.3(MSH6):c.3961A>G (p.Arg1321Gly)	rs41295278	0.00019
NM_000179.3(MSH6):c.2398G>C (p.Val800Leu)	rs61748083	0.00014
NM_000179.3(MSH6):c.3203G>A (p.Arg1068Gln)	rs398123230	0.00012
NM_000179.3(MSH6):c.942C>G (p.Ser314Arg)	rs150440246	0.00011
NM_000179.3(MSH6):c.335A>G (p.Asn112Ser)	rs587779934	0.00010
NM_000179.3(MSH6):c.1730G>A (p.Arg577His)	rs376220212	0.00009
NM_000179.3(MSH6):c.643G>A (p.Val215Ile)	rs145959653	0.00006
NM_000179.3(MSH6):c.2347T>A (p.Cys783Ser)	rs373721483	0.00005
NM_000179.3(MSH6):c.749T>C (p.Val250Ala)	rs587781275	0.00004
NM_000179.3(MSH6):c.2156C>T (p.Thr719Ile)	rs373418713	0.00003
NM_000179.3(MSH6):c.359T>C (p.Ile120Thr)	rs775971872	0.00003
NM_000179.3(MSH6):c.728G>A (p.Arg243His)	rs370157832	0.00002
NM_000179.3(MSH6):c.1061G>T (p.Gly354Val)	rs730881788	0.00001
NM_000179.3(MSH6):c.188C>G (p.Ser63Cys)	rs587779920	0.00001
NM_000179.3(MSH6):c.2001T>A (p.Asp667Glu)	rs1361745058	0.00001
NM_000179.3(MSH6):c.2385A>G (p.Ile795Met)	rs1558665293	0.00001
NM_000179.3(MSH6):c.2588A>G (p.Glu863Gly)	rs876658238	0.00001
NM_000179.3(MSH6):c.3334G>A (p.Asp1112Asn)	rs773955368	0.00001
NM_000179.3(MSH6):c.998C>T (p.Thr333Ile)	rs587781983	0.00001
NM_000179.3(MSH6):c.1111G>C (p.Glu371Gln)
NM_000179.3(MSH6):c.1602C>G (p.Asn534Lys)	rs763712971
NM_000179.3(MSH6):c.1657A>C (p.Thr553Pro)	rs1294509946
NM_000179.3(MSH6):c.1666T>C (p.Tyr556His)	rs1060502895
NM_000179.3(MSH6):c.1847C>G (p.Ser616Cys)	rs772363120
NM_000179.3(MSH6):c.261-6C>G	rs1558651835
NM_000179.3(MSH6):c.3259C>T (p.Pro1087Ser)	rs63750998
NM_000179.3(MSH6):c.3450A>C (p.Leu1150Phe)	rs762134820
NM_000179.3(MSH6):c.382C>T (p.Arg128Cys)	rs1251938412
NM_000179.3(MSH6):c.439C>T (p.Leu147Phe)	rs2104111618
NM_000179.3(MSH6):c.503C>T (p.Ala168Val)	rs774162322
NM_000179.3(MSH6):c.866_867delinsAA (p.Gly289Glu)	rs267608079
NM_000179.3(MSH6):c.905G>C (p.Arg302Thr)	rs587781510

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