List of variants in gene MSH6 reported as uncertain significance by University of Washington Department of Laboratory Medicine, University of Washington

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: 46

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3217C>T (p.Pro1073Ser)	rs142254875	0.00028
NM_000179.3(MSH6):c.73G>T (p.Ala25Ser)	rs267608026	0.00023
NM_000179.3(MSH6):c.2398G>C (p.Val800Leu)	rs61748083	0.00014
NM_000179.3(MSH6):c.884A>G (p.Lys295Arg)	rs267608051	0.00014
NM_000179.3(MSH6):c.3203G>A (p.Arg1068Gln)	rs398123230	0.00012
NM_000179.3(MSH6):c.3283C>T (p.Arg1095Cys)	rs376243329	0.00006
NM_000179.3(MSH6):c.1364A>C (p.Asn455Thr)	rs200938360	0.00004
NM_000179.3(MSH6):c.1402C>T (p.Arg468Cys)	rs369456858	0.00004
NM_000179.3(MSH6):c.1915G>A (p.Glu639Lys)	rs143517321	0.00003
NM_000179.3(MSH6):c.1082G>A (p.Arg361His)	rs63750440	0.00002
NM_000179.3(MSH6):c.2315G>A (p.Arg772Gln)	rs63750725	0.00002
NM_000179.3(MSH6):c.2701C>A (p.Arg901Ser)	rs772514245	0.00002
NM_000179.3(MSH6):c.1106C>T (p.Thr369Ile)	rs375974046	0.00001
NM_000179.3(MSH6):c.1599G>C (p.Glu533Asp)	rs373726731	0.00001
NM_000179.3(MSH6):c.2210C>T (p.Ala737Val)	rs869312798	0.00001
NM_000179.3(MSH6):c.2876G>A (p.Arg959His)	rs757653982	0.00001
NM_000179.3(MSH6):c.3227G>A (p.Arg1076His)	rs779617676	0.00001
NM_000179.3(MSH6):c.44C>T (p.Pro15Leu)	rs869312800	0.00001
NM_000179.3(MSH6):c.1046A>G (p.Gln349Arg)	rs869312797
NM_000179.3(MSH6):c.1093T>C (p.Trp365Arg)	rs752628520
NM_000179.3(MSH6):c.1184C>T (p.Thr395Ile)	rs767658494
NM_000179.3(MSH6):c.1290G>A (p.Gly430=)	rs1558661242
NM_000179.3(MSH6):c.1401C>T (p.Gly467=)	rs1558661556
NM_000179.3(MSH6):c.1675T>C (p.Cys559Arg)	rs1558662565
NM_000179.3(MSH6):c.1754T>C (p.Leu585Pro)	rs587779220
NM_000179.3(MSH6):c.1847C>G (p.Ser616Cys)	rs772363120
NM_000179.3(MSH6):c.2161A>C (p.Arg721=)	rs537604099
NM_000179.3(MSH6):c.2195G>A (p.Arg732Gln)	rs749746725
NM_000179.3(MSH6):c.2287G>A (p.Asp763Asn)	rs1558664969
NM_000179.3(MSH6):c.2636C>A (p.Ala879Asp)	rs1558666061
NM_000179.3(MSH6):c.2660T>C (p.Leu887Pro)	rs1558666142
NM_000179.3(MSH6):c.2743G>A (p.Ala915Thr)	rs1558666565
NM_000179.3(MSH6):c.2743G>T (p.Ala915Ser)	rs1558666565
NM_000179.3(MSH6):c.3010A>G (p.Lys1004Glu)	rs1558667702
NM_000179.3(MSH6):c.3139T>C (p.Trp1047Arg)	rs1114167753
NM_000179.3(MSH6):c.3214G>A (p.Gly1072Ser)	rs1558386938
NM_000179.3(MSH6):c.3438+2T>C	rs1033749344
NM_000179.3(MSH6):c.3442G>A (p.Gly1148Ser)	rs63750257
NM_000179.3(MSH6):c.3470G>A (p.Gly1157Asp)	rs752212361
NM_000179.3(MSH6):c.3508A>C (p.Ile1170Leu)	rs1558389423
NM_000179.3(MSH6):c.3610G>A (p.Ala1204Thr)	rs869312799
NM_000179.3(MSH6):c.3963A>G (p.Arg1321=)	rs267608125
NM_000179.3(MSH6):c.457G>T (p.Gly153Cys)	rs1060502885
NM_000179.3(MSH6):c.556G>T (p.Asp186Tyr)	rs1212607928
NM_000179.3(MSH6):c.884A>T (p.Lys295Ile)	rs267608051
NM_000179.3(MSH6):c.893G>A (p.Arg298Gln)	rs765237563

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