List of variants in gene MLH1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 38

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.1166G>A (p.Arg389Gln)	rs63750361	0.00020
NM_000249.4(MLH1):c.65G>C (p.Gly22Ala)	rs41295280	0.00016
NM_000249.3(MLH1):c.-42C>T	rs41285097	0.00009
NM_000249.4(MLH1):c.1558+5G>A	rs199935667	0.00008
NM_000249.4(MLH1):c.1013A>G (p.Asn338Ser)	rs63751467	0.00006
NM_000249.4(MLH1):c.1360G>C (p.Gly454Arg)	rs63750527	0.00006
NM_000249.4(MLH1):c.2174G>A (p.Arg725His)	rs566928243	0.00006
NM_000249.4(MLH1):c.955G>A (p.Glu319Lys)	rs63750796	0.00006
NM_000249.4(MLH1):c.1153C>T (p.Arg385Cys)	rs63750760	0.00005
NM_000249.4(MLH1):c.1154G>A (p.Arg385His)	rs63750430	0.00005
NM_000249.4(MLH1):c.299G>A (p.Arg100Gln)	rs63750266	0.00004
NM_000249.4(MLH1):c.347C>A (p.Thr116Lys)	rs63750465	0.00004
NM_000249.4(MLH1):c.1051G>A (p.Gly351Arg)	rs1437454428	0.00003
NM_000249.4(MLH1):c.1730C>T (p.Ser577Leu)	rs56185292	0.00003
NM_000249.4(MLH1):c.226G>A (p.Val76Ile)	rs878853788	0.00002
NM_000249.4(MLH1):c.1118G>A (p.Gly373Glu)	rs774878513	0.00001
NM_000249.4(MLH1):c.1243G>A (p.Asp415Asn)	rs373767220	0.00001
NM_000249.4(MLH1):c.1344G>T (p.Glu448Asp)	rs587779952	0.00001
NM_000249.4(MLH1):c.1896+5G>A	rs759870594	0.00001
NM_000249.4(MLH1):c.2162A>G (p.Tyr721Cys)	rs587778986	0.00001
NM_000249.4(MLH1):c.2254G>C (p.Val752Leu)	rs1196350669	0.00001
NM_000249.4(MLH1):c.650G>A (p.Arg217His)	rs762099920	0.00001
NM_000249.4(MLH1):c.821A>G (p.Lys274Arg)	rs769958855	0.00001
NM_000249.4(MLH1):c.1039-3C>G	rs730881737
NM_000249.4(MLH1):c.1117G>A (p.Gly373Arg)	rs766904735
NM_000249.4(MLH1):c.1487C>G (p.Pro496Arg)	rs63750226
NM_000249.4(MLH1):c.1572G>T (p.Met524Ile)	rs587779953
NM_000249.4(MLH1):c.1775G>A (p.Ser592Asn)	rs587782621
NM_000249.4(MLH1):c.185A>G (p.Gln62Arg)	rs2081171469
NM_000249.4(MLH1):c.2042C>T (p.Ala681Val)	rs63750864
NM_000249.4(MLH1):c.229T>G (p.Cys77Gly)	rs63749859
NM_000249.4(MLH1):c.242C>G (p.Thr81Ser)	rs63751069
NM_000249.4(MLH1):c.53G>A (p.Arg18His)	rs1553637254
NM_000249.4(MLH1):c.553G>A (p.Val185Ile)	rs63750012
NM_000249.4(MLH1):c.726G>A (p.Met242Ile)	rs1559534445
NM_000249.4(MLH1):c.844G>A (p.Ala282Thr)	rs774689817
NM_000249.4(MLH1):c.91G>A (p.Ala31Thr)	rs749671520
NM_000249.4(MLH1):c.91_92delinsTG (p.Ala31Cys)	rs63749994

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