List of variants in gene MSH2 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.965G>A (p.Gly322Asp)	rs4987188	0.01714
NM_000251.3(MSH2):c.942+3A>T	rs193922376	0.00072
NM_000251.3(MSH2):c.435T>G (p.Ile145Met)	rs63750124	0.00031
NM_000251.3(MSH2):c.1386+23T>G	rs747646424	0.00010
NM_000251.3(MSH2):c.4G>A (p.Ala2Thr)	rs63750466	0.00008
NM_000251.3(MSH2):c.1571G>A (p.Arg524His)	rs63751207	0.00001
NM_000251.3(MSH2):c.1661+3T>G	rs1064793688
NM_000251.3(MSH2):c.1861C>T (p.Arg621Ter)	rs63750508
NM_000251.3(MSH2):c.2029A>G (p.Thr677Ala)	rs1553369013
NM_000251.3(MSH2):c.204del (p.Pro69fs)	rs63750199
NM_000251.3(MSH2):c.229_230del (p.Ser77fs)	rs63749848
NM_000251.3(MSH2):c.2697G>T (p.Met899Ile)	rs878853813
NM_000251.3(MSH2):c.482T>C (p.Val161Ala)	rs63750126
NM_000251.3(MSH2):c.942+14_942+29del	rs11309117
NM_000251.3(MSH2):c.942+22_942+29del	rs11309117
NM_000251.3(MSH2):c.942+26_942+29del	rs11309117

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