List of variants in gene MSH6 reported as uncertain significance for adenocarcinoma

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

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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.3438+11_3438+14del	rs377746844	0.00023
NM_000179.3(MSH6):c.3245C>T (p.Pro1082Leu)	rs191109849	0.00010
NM_000179.3(MSH6):c.1730G>A (p.Arg577His)	rs376220212	0.00009
NM_000179.3(MSH6):c.3727A>T (p.Thr1243Ser)	rs147453999	0.00009
NM_000179.3(MSH6):c.1474A>G (p.Met492Val)	rs61754783	0.00008
NM_000179.3(MSH6):c.147C>T (p.Ala49=)	rs768803986	0.00005
NM_000179.3(MSH6):c.2889C>T (p.Gly963=)	rs771726914	0.00002
NM_000179.3(MSH6):c.3851C>T (p.Thr1284Met)	rs63750836	0.00002
NM_000179.3(MSH6):c.628-8C>T	rs767991179	0.00002
NM_000179.3(MSH6):c.2926C>T (p.Arg976Cys)	rs587782386	0.00001
NM_000179.3(MSH6):c.3172+14C>T	rs762990595	0.00001
NM_000179.3(MSH6):c.1196C>T (p.Pro399Leu)	rs878853701
NM_000179.3(MSH6):c.1553C>A (p.Thr518Asn)	rs1553412945
NM_000179.3(MSH6):c.1600A>G (p.Asn534Asp)	rs1669350157
NM_000179.3(MSH6):c.1667A>G (p.Tyr556Cys)	rs63751312
NM_000179.3(MSH6):c.167G>T (p.Gly56Val)	rs1572698275
NM_000179.3(MSH6):c.1712G>A (p.Gly571Asp)	rs863224618
NM_000179.3(MSH6):c.1750A>C (p.Thr584Pro)	rs1553413123
NM_000179.3(MSH6):c.1996T>C (p.Ser666Pro)	rs587779222
NM_000179.3(MSH6):c.2108T>C (p.Met703Thr)	rs1064793189
NM_000179.3(MSH6):c.2905T>C (p.Tyr969His)	rs1348956744
NM_000179.3(MSH6):c.2936T>C (p.Leu979Pro)	rs1218426245
NM_000179.3(MSH6):c.2989A>G (p.Lys997Glu)	rs1064794943
NM_000179.3(MSH6):c.3079G>C (p.Val1027Leu)	rs876658397
NM_000179.3(MSH6):c.3151_3152dup (p.Val1051_Glu1052insTer)	rs1175196087
NM_000179.3(MSH6):c.3172G>C (p.Asp1058His)	rs863225404
NM_000179.3(MSH6):c.334A>G (p.Asn112Asp)	rs864622397
NM_000179.3(MSH6):c.3644T>A (p.Leu1215Ter)	rs2104526529
NM_000179.3(MSH6):c.3801+3A>G	rs753049136
NM_000179.3(MSH6):c.3946G>A (p.Gly1316Arg)	rs773675555
NM_000179.3(MSH6):c.3971AGA[1] (p.Lys1325del)	rs587779300
NM_000179.3(MSH6):c.513A>G (p.Glu171=)	rs786201116
NM_000179.3(MSH6):c.818G>A (p.Gly273Glu)	rs769610487

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