List of variants in gene MSH2 reported by Cancer Genomics Group, Japanese Foundation For Cancer Research

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.1255C>A (p.Gln419Lys)	rs63750006	0.00019
NM_000251.3(MSH2):c.2425G>A (p.Glu809Lys)	rs202145681	0.00013
NM_000251.3(MSH2):c.505A>G (p.Ile169Val)	rs63750716	0.00013
NM_000251.3(MSH2):c.14C>A (p.Pro5Gln)	rs56170584	0.00003
NM_000251.3(MSH2):c.118G>A (p.Gly40Ser)	rs63751260	0.00001
NM_000251.3(MSH2):c.2064G>A (p.Met688Ile)	rs63750790	0.00001
NM_000251.3(MSH2):c.2407A>G (p.Thr803Ala)	rs63751168	0.00001
NM_000251.3(MSH2):c.266T>C (p.Val89Ala)	rs876659747	0.00001
NM_000251.3(MSH2):c.1315C>G (p.Pro439Ala)	rs786203116
NM_000251.3(MSH2):c.1501A>G (p.Arg501Gly)	rs1666734097
NM_000251.3(MSH2):c.1638G>C (p.Lys546Asn)	rs372350768
NM_000251.3(MSH2):c.1846C>T (p.Pro616Ser)	rs587782627
NM_000251.3(MSH2):c.2209A>G (p.Arg737Gly)	rs1573570754
NM_000251.3(MSH2):c.2533A>G (p.Lys845Glu)	rs63750571
NM_000251.3(MSH2):c.448G>T (p.Val150Phe)	rs1558459157

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