List of variants in gene MLH1 reported as not provided for not provided

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.885-81G>C	rs104894999	0.02021
NM_000249.4(MLH1):c.588+11G>C	rs4647258	0.00993
NM_000249.4(MLH1):c.791-79A>G	rs104894998	0.00459
NM_000249.4(MLH1):c.545+20A>T	rs121909453	0.00424
NM_000249.4(MLH1):c.1852A>G (p.Lys618Glu)	rs35001569	0.00399
NM_000249.4(MLH1):c.-7C>T	rs104894994	0.00115
NM_000249.4(MLH1):c.-28A>G	rs56198082	0.00110
NM_000249.4(MLH1):c.117-109A>G	rs104894995	0.00025
NM_000249.4(MLH1):c.307-19A>G	rs121909451	0.00022
NM_000249.4(MLH1):c.545+19G>T	rs41285099	0.00007
NM_000249.3(MLH1):c.-32C>G	rs1016433173	0.00006
NM_000249.4(MLH1):c.207+12C>T	rs121909450	0.00006
NM_000249.4(MLH1):c.955G>A (p.Glu319Lys)	rs63750796	0.00006
NM_000249.4(MLH1):c.1148T>C (p.Met383Thr)	rs141344760	0.00004
NM_000249.4(MLH1):c.2162A>G (p.Tyr721Cys)	rs587778986	0.00001
NM_000249.4(MLH1):c.739T>G (p.Ser247Ala)	rs63750948	0.00001
NM_000249.4(MLH1):c.-27C>T	rs587779001
NM_000249.4(MLH1):c.1039-6A>T	rs1131692027
NM_000249.4(MLH1):c.1154G>C (p.Arg385Pro)	rs63750430
NM_000249.4(MLH1):c.1226A>C (p.Gln409Pro)	rs104895000
NM_000249.4(MLH1):c.1668-35G>A	rs104895001
NM_000249.4(MLH1):c.1853A>C (p.Lys618Thr)	rs63750449
NM_000249.4(MLH1):c.1912G>A (p.Gly638Arg)	rs63750549
NM_000249.4(MLH1):c.2180A>T (p.His727Leu)	rs104895002
NM_000249.4(MLH1):c.380+16C>G	rs121909452
NM_000249.4(MLH1):c.788A>C (p.Asn263Thr)	rs104894997

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