List of variants in gene MSH2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.1666T>C (p.Leu556=)	rs61756466	0.00471
NM_000251.3(MSH2):c.339G>A (p.Lys113=)	rs35898375	0.00313
NM_000251.3(MSH2):c.*226A>G	rs17225060	0.00201
NM_000251.3(MSH2):c.1387-8G>T	rs187525243	0.00143
NM_000251.3(MSH2):c.1737A>G (p.Lys579=)	rs61756467	0.00138
NM_000251.3(MSH2):c.1759+57G>T	rs17218363	0.00089
NM_000251.3(MSH2):c.1563T>C (p.Tyr521=)	rs63750330	0.00053
NM_000251.3(MSH2):c.1680T>C (p.Asn560=)	rs200056411	0.00043
NM_000251.3(MSH2):c.2154A>G (p.Gln718=)	rs63750810	0.00033
NM_000251.3(MSH2):c.435T>G (p.Ile145Met)	rs63750124	0.00031
NM_000251.3(MSH2):c.471C>A (p.Gly157=)	rs61756463	0.00029
NM_000251.3(MSH2):c.1787A>G (p.Asn596Ser)	rs41295288	0.00022
NM_000251.3(MSH2):c.1748A>G (p.Asn583Ser)	rs201118107	0.00014
NM_000251.3(MSH2):c.1386+23T>G	rs747646424	0.00010
NM_000251.3(MSH2):c.2802G>A (p.Thr934=)	rs150259097	0.00009
NM_000251.3(MSH2):c.1560A>G (p.Gly520=)	rs63750820	0.00007
NM_000251.3(MSH2):c.2400A>G (p.Leu800=)	rs201298777	0.00006
NM_000251.3(MSH2):c.211+8C>T	rs267607916	0.00003
NM_000251.3(MSH2):c.1131A>G (p.Gln377=)	rs181852377	0.00002
NM_000251.3(MSH2):c.1764T>C (p.Tyr588=)	rs63750844	0.00002
NM_000251.3(MSH2):c.2061C>G (p.Leu687=)	rs63750032	0.00002
NM_000251.3(MSH2):c.438T>C (p.Gly146=)	rs587779161	0.00002
NM_000251.3(MSH2):c.105C>A (p.Arg35=)	rs775554736	0.00001
NM_000251.3(MSH2):c.1194A>G (p.Ala398=)	rs1060504412	0.00001
NM_000251.3(MSH2):c.2190G>A (p.Leu730=)	rs864622370	0.00001
NM_000251.3(MSH2):c.1277-3127A>G
NM_000251.3(MSH2):c.1277-3128TA[6]
NM_000251.3(MSH2):c.2088A>G (p.Pro696=)	rs878853807
NM_000251.3(MSH2):c.2268C>G (p.Thr756=)	rs1404389752
NM_000251.3(MSH2):c.498G>C (p.Val166=)
NM_000251.3(MSH2):c.507A>G (p.Ile169Met)	rs748762580
NM_000251.3(MSH2):c.6G>C (p.Ala2=)	rs368270856
NM_000251.3(MSH2):c.965G>T (p.Gly322Val)	rs4987188

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