List of variants in gene MSH6 studied for Breast carcinoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.116G>A (p.Gly39Glu)	rs1042821	0.18742
NM_000179.3(MSH6):c.3160A>T (p.Ile1054Phe)	rs267608075	0.00016
NM_000179.3(MSH6):c.3226C>T (p.Arg1076Cys)	rs63750617	0.00002
NM_000179.3(MSH6):c.2731C>T (p.Arg911Ter)	rs63751017	0.00001
NM_000179.3(MSH6):c.3893A>G (p.Tyr1298Cys)	rs786202520	0.00001
NM_000179.3(MSH6):c.1572_1573del (p.Tyr524_Ser525delinsTer)	rs1114167702
NM_000179.3(MSH6):c.3259C>T (p.Pro1087Ser)	rs63750998
NM_000179.3(MSH6):c.3732_3735dup (p.Ser1246fs)	rs1553333072
NM_000179.3(MSH6):c.3969T>G (p.Phe1323Leu)	rs1057520473

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