List of variants in gene MSH6 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.2561A>T (p.Lys854Met)	rs34374438	0.00036
NM_000179.3(MSH6):c.4002-10T>A	rs545466048	0.00026
NM_000179.3(MSH6):c.884A>G (p.Lys295Arg)	rs267608051	0.00014
NM_000179.3(MSH6):c.3727A>T (p.Thr1243Ser)	rs147453999	0.00009
NM_000179.3(MSH6):c.3283C>T (p.Arg1095Cys)	rs376243329	0.00006
NM_000179.3(MSH6):c.3824G>A (p.Cys1275Tyr)	rs150990541	0.00006
NM_000179.3(MSH6):c.1661G>A (p.Arg554His)	rs730881791	0.00004
NM_000179.3(MSH6):c.-8C>T	rs565211544	0.00003
NM_000179.3(MSH6):c.3303G>T (p.Lys1101Asn)	rs370353868	0.00003
NM_000179.3(MSH6):c.3543C>G (p.Asp1181Glu)	rs267608100	0.00003
NM_000179.3(MSH6):c.1082G>A (p.Arg361His)	rs63750440	0.00002
NM_000179.3(MSH6):c.2092C>G (p.Gln698Glu)	rs63750832	0.00002
NM_000179.3(MSH6):c.2258C>G (p.Ser753Cys)	rs876660934	0.00002
NM_000179.3(MSH6):c.241G>A (p.Ala81Thr)	rs587779239	0.00001
NM_000179.3(MSH6):c.3313G>A (p.Gly1105Arg)	rs755716475	0.00001
NM_000179.3(MSH6):c.3592G>A (p.Ala1198Thr)	rs1669962346	0.00001
NM_000179.3(MSH6):c.361C>T (p.Arg121Cys)	rs763593669	0.00001
NM_000179.3(MSH6):c.3919A>G (p.Asn1307Asp)	rs730881808	0.00001
NM_000179.3(MSH6):c.40T>G (p.Ser14Ala)	rs876660417	0.00001
NM_000179.3(MSH6):c.23_26dup
NM_000179.3(MSH6):c.1435A>G (p.Lys479Glu)
NM_000179.3(MSH6):c.1477G>A (p.Glu493Lys)	rs267608046
NM_000179.3(MSH6):c.1712G>A (p.Gly571Asp)	rs863224618
NM_000179.3(MSH6):c.1906A>G (p.Thr636Ala)
NM_000179.3(MSH6):c.1998T>A (p.Ser666=)	rs1553413364
NM_000179.3(MSH6):c.2288A>C (p.Asp763Ala)	rs1060502913
NM_000179.3(MSH6):c.2413A>G (p.Ile805Val)	rs928923556
NM_000179.3(MSH6):c.2491C>G (p.Pro831Ala)	rs267608053
NM_000179.3(MSH6):c.2590G>A (p.Gly864Arg)	rs1669485106
NM_000179.3(MSH6):c.2687A>T (p.Lys896Ile)	rs876658369
NM_000179.3(MSH6):c.2698G>T (p.Gly900Cys)
NM_000179.3(MSH6):c.2824G>A (p.Ala942Thr)
NM_000179.3(MSH6):c.3286C>T (p.His1096Tyr)	rs1553331471
NM_000179.3(MSH6):c.3613A>G (p.Thr1205Ala)	rs1064797252
NM_000179.3(MSH6):c.3716_3736dup (p.Phe1245_Ser1246insLeuLysCysArgThrLeuPhe)	rs1670049545
NM_000179.3(MSH6):c.3997_4001+63dup

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