List of variants in gene MLH1 reported as likely benign for carcinoma

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.2152C>T (p.His718Tyr)	rs2020873	0.02345
NM_000249.4(MLH1):c.1963A>G (p.Ile655Val)	rs55907433	0.00297
NM_000249.4(MLH1):c.-7C>T	rs104894994	0.00115
NM_000249.4(MLH1):c.803A>G (p.Glu268Gly)	rs63750650	0.00014
NM_000249.4(MLH1):c.649C>T (p.Arg217Cys)	rs4986984	0.00007
NM_000249.4(MLH1):c.438A>G (p.Gln146=)	rs377279035	0.00005
NM_000249.4(MLH1):c.2252A>G (p.Lys751Arg)	rs140195825	0.00004
NM_000249.4(MLH1):c.2103+6G>T	rs1057521607	0.00001
NM_000249.4(MLH1):c.1039-8_1039-7insTA	rs535965616
NM_000249.4(MLH1):c.1573T>C (p.Leu525=)	rs63750137
NM_000249.4(MLH1):c.1852_1853delinsGC (p.Lys618Ala)	rs35502531

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