List of variants in gene MSH6 reported as likely benign 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: 49

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.1186C>G (p.Leu396Val)	rs2020908	0.00565
NM_000179.3(MSH6):c.2633T>C (p.Val878Ala)	rs2020912	0.00448
NM_000179.3(MSH6):c.4001+39C>G	rs201482798	0.00112
NM_000179.3(MSH6):c.984C>T (p.Ser328=)	rs138143769	0.00101
NM_000179.3(MSH6):c.1526T>C (p.Val509Ala)	rs63751005	0.00067
NM_000179.3(MSH6):c.1665A>G (p.Ala555=)	rs146785465	0.00066
NM_000179.3(MSH6):c.663A>C (p.Glu221Asp)	rs41557217	0.00064
NM_000179.3(MSH6):c.1508C>G (p.Ser503Cys)	rs63750897	0.00059
NM_000179.3(MSH6):c.1449G>T (p.Val483=)	rs35590297	0.00037
NM_000179.3(MSH6):c.3488A>T (p.Glu1163Val)	rs63750252	0.00032
NM_000179.3(MSH6):c.3217C>T (p.Pro1073Ser)	rs142254875	0.00028
NM_000179.3(MSH6):c.49_68dup	rs777409019	0.00021
NM_000179.3(MSH6):c.3160A>T (p.Ile1054Phe)	rs267608075	0.00016
NM_000179.3(MSH6):c.3203G>A (p.Arg1068Gln)	rs398123230	0.00012
NM_000179.3(MSH6):c.1875C>T (p.Ser625=)	rs63749886	0.00010
NM_000179.3(MSH6):c.3024C>T (p.Thr1008=)	rs587780675	0.00009
NM_000179.3(MSH6):c.660A>C (p.Glu220Asp)	rs1800938	0.00009
NM_000179.3(MSH6):c.1050C>T (p.Ala350=)	rs730881802	0.00006
NM_000179.3(MSH6):c.178T>C (p.Leu60=)	rs35819209	0.00006
NM_000179.3(MSH6):c.3986C>T (p.Ser1329Leu)	rs199594809	0.00006
NM_000179.3(MSH6):c.926C>G (p.Ser309Cys)	rs544222338	0.00006
NM_000179.3(MSH6):c.2239C>T (p.Leu747=)	rs63751305	0.00005
NM_000179.3(MSH6):c.107C>T (p.Ala36Val)	rs61756469	0.00004
NM_000179.3(MSH6):c.2904C>G (p.Val968=)	rs150683226	0.00004
NM_000179.3(MSH6):c.3729A>G (p.Thr1243=)	rs773807182	0.00004
NM_000179.3(MSH6):c.2319C>T (p.Leu773=)	rs63749895	0.00003
NM_000179.3(MSH6):c.627+9C>T	rs373155872	0.00003
NM_000179.3(MSH6):c.1773A>G (p.Pro591=)	rs752239740	0.00002
NM_000179.3(MSH6):c.1170T>C (p.Asp390=)	rs55882234	0.00001
NM_000179.3(MSH6):c.2154C>T (p.Ser718=)	rs771662801	0.00001
NM_000179.3(MSH6):c.2400T>C (p.Val800=)	rs267608071	0.00001
NM_000179.3(MSH6):c.3300G>A (p.Thr1100=)	rs540252208	0.00001
NM_000179.3(MSH6):c.3936T>C (p.Val1312=)	rs61753796	0.00001
NM_000179.3(MSH6):c.980C>G (p.Thr327Ser)	rs369568820	0.00001
MHS6:c.3647-65_3647-61del	rs3136363
NM_000179.3(MSH6):c.-6G>T	rs730881822
NM_000179.3(MSH6):c.1167C>G (p.Pro389=)	rs1042819
NM_000179.3(MSH6):c.2187C>T (p.Ala729=)	rs375610656
NM_000179.3(MSH6):c.2322A>G (p.Leu774=)	rs1057521386
NM_000179.3(MSH6):c.3246G>A (p.Pro1082=)	rs3136351
NM_000179.3(MSH6):c.3246G>T (p.Pro1082=)	rs3136351
NM_000179.3(MSH6):c.3259C>G (p.Pro1087Ala)	rs63750998
NM_000179.3(MSH6):c.369A>G (p.Lys123=)
NM_000179.3(MSH6):c.3758T>A (p.Val1253Glu)	rs202066386
NM_000179.3(MSH6):c.4001+2TAAC[2]	rs267608132
NM_000179.3(MSH6):c.4001+2TAAC[4]	rs267608132
NM_000179.3(MSH6):c.4083GACT[3] (p.Ter1361=)	rs765313977
NM_000179.3(MSH6):c.432C>T (p.Ser144=)	rs1046304919
NM_000179.3(MSH6):c.501T>C (p.Ser167=)	rs1572716201

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