ClinVar Miner

List of variants studied for Turcot syndrome; Muir-Torré syndrome; Lynch syndrome II by Fulgent Genetics,Fulgent Genetics

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Total variants: 36
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HGVS dbSNP
NM_000249.3(MLH1):c.1039-3C>G rs730881737
NM_000249.3(MLH1):c.1118G>A (p.Gly373Glu) rs774878513
NM_000249.3(MLH1):c.1243G>A (p.Asp415Asn) rs373767220
NM_000249.3(MLH1):c.1459C>T (p.Arg487Ter) rs63749795
NM_000249.3(MLH1):c.1487C>G (p.Pro496Arg) rs63750226
NM_000249.3(MLH1):c.1558+5G>A rs199935667
NM_000249.3(MLH1):c.1572G>T (p.Met524Ile) rs587779953
NM_000249.3(MLH1):c.1730C>T (p.Ser577Leu) rs56185292
NM_000249.3(MLH1):c.1775G>A (p.Ser592Asn) rs587782621
NM_000249.3(MLH1):c.1896+5G>A rs759870594
NM_000249.3(MLH1):c.1897-2A>G rs267607871
NM_000249.3(MLH1):c.2041G>A (p.Ala681Thr) rs63750217
NM_000249.3(MLH1):c.2042C>T (p.Ala681Val) rs63750864
NM_000249.3(MLH1):c.2059C>T (p.Arg687Trp) rs63751275
NM_000249.3(MLH1):c.208-3C>G rs267607720
NM_000249.3(MLH1):c.2174G>A (p.Arg725His) rs566928243
NM_000249.3(MLH1):c.226G>A (p.Val76Ile) rs878853788
NM_000249.3(MLH1):c.299G>A (p.Arg100Gln) rs63750266
NM_000249.3(MLH1):c.306+5G>A rs267607735
NM_000249.3(MLH1):c.347C>A (p.Thr116Lys) rs63750465
NM_000249.3(MLH1):c.588+5G>A rs267607768
NM_000249.3(MLH1):c.821A>G (p.Lys274Arg) rs769958855
NM_000249.3(MLH1):c.844G>A (p.Ala282Thr) rs774689817
NM_000249.3(MLH1):c.885-1G>A rs1553647894
NM_000249.3(MLH1):c.91G>A (p.Ala31Thr) rs749671520
NM_000249.3(MLH1):c.955G>A (p.Glu319Lys) rs63750796
NM_000249.4(MLH1):c.1013A>G (p.Asn338Ser) rs63751467
NM_000249.4(MLH1):c.1117G>A (p.Gly373Arg) rs766904735
NM_000249.4(MLH1):c.1151T>A (p.Val384Asp) rs63750447
NM_000249.4(MLH1):c.1153C>T (p.Arg385Cys) rs63750760
NM_000249.4(MLH1):c.1154G>A (p.Arg385His) rs63750430
NM_000249.4(MLH1):c.1166G>A (p.Arg389Gln) rs63750361
NM_000249.4(MLH1):c.1360G>C (p.Gly454Arg) rs63750527
NM_000249.4(MLH1):c.1381A>T (p.Lys461Ter) rs63750540
NM_000249.4(MLH1):c.65G>C (p.Gly22Ala) rs41295280
NM_001167617.2(MLH1):c.-426_-425delinsTG rs63749994

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