List of variants in gene MSH6 reported as uncertain significance for mismatch repair cancer syndrome 1

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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: 32

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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.3217C>T (p.Pro1073Ser)	rs142254875	0.00028
NM_000179.3(MSH6):c.73G>T (p.Ala25Ser)	rs267608026	0.00023
NM_000179.3(MSH6):c.187T>C (p.Ser63Pro)	rs763702846	0.00013
NM_000179.3(MSH6):c.3788G>A (p.Arg1263His)	rs147852216	0.00010
NM_000179.3(MSH6):c.1063G>A (p.Gly355Ser)	rs587778531	0.00009
NM_000179.3(MSH6):c.1814C>G (p.Thr605Ser)	rs587781616	0.00006
NM_000179.3(MSH6):c.3163G>A (p.Ala1055Thr)	rs587779254	0.00002
NM_000179.3(MSH6):c.3244C>T (p.Pro1082Ser)	rs186240214	0.00002
NM_000179.3(MSH6):c.3557G>A (p.Gly1186Asp)	rs587781690	0.00002
NM_000179.3(MSH6):c.136G>A (p.Gly46Arg)	rs863224616	0.00001
NM_000179.3(MSH6):c.1633A>G (p.Lys545Glu)	rs1064793403	0.00001
NM_000179.3(MSH6):c.2300C>G (p.Thr767Ser)	rs587781462	0.00001
NM_000179.3(MSH6):c.2419G>A (p.Glu807Lys)	rs587779923	0.00001
NM_000179.3(MSH6):c.2515G>C (p.Asp839His)	rs1553413868	0.00001
NM_000179.3(MSH6):c.2959A>G (p.Thr987Ala)	rs746631156	0.00001
NM_000179.3(MSH6):c.3014G>A (p.Arg1005Gln)	rs587782324	0.00001
NM_000179.3(MSH6):c.3312T>A (p.Phe1104Leu)	rs747441460	0.00001
NM_000179.3(MSH6):c.3605T>C (p.Met1202Thr)	rs587779273	0.00001
NM_000179.3(MSH6):c.4043A>C (p.Glu1348Ala)	rs1449733937	0.00001
NM_000179.3(MSH6):c.104C>T (p.Ala35Val)	rs776547943
NM_000179.3(MSH6):c.1270G>A (p.Val424Ile)	rs768299607
NM_000179.3(MSH6):c.136G>C (p.Gly46Arg)	rs863224616
NM_000179.3(MSH6):c.184C>T (p.Arg62Cys)	rs876659508
NM_000179.3(MSH6):c.2183A>G (p.Lys728Arg)	rs35552856
NM_000179.3(MSH6):c.3259C>T (p.Pro1087Ser)	rs63750998
NM_000179.3(MSH6):c.3260C>A (p.Pro1087His)	rs63750753
NM_000179.3(MSH6):c.3260C>G (p.Pro1087Arg)	rs63750753
NM_000179.3(MSH6):c.3299C>T (p.Thr1100Met)	rs63750442
NM_000179.3(MSH6):c.383G>T (p.Arg128Leu)	rs63750143
NM_000179.3(MSH6):c.3919A>C (p.Asn1307His)	rs730881808
NM_000179.3(MSH6):c.622A>G (p.Met208Val)	rs369058374

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