ClinVar Miner

List of variants in gene TMEM237 reported by Preventiongenetics, part of Exact Sciences

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001044385.3(TMEM237):c.274+23A>G rs1208081 0.64988
NM_001044385.3(TMEM237):c.1037+49C>T rs2540450 0.29727
NM_001044385.3(TMEM237):c.1096G>T (p.Ala366Ser) rs73989521 0.07946
NM_001044385.3(TMEM237):c.75-13T>C rs116829037 0.00764
NM_001044385.3(TMEM237):c.554-15G>A rs144051344 0.00213
NM_001044385.3(TMEM237):c.1134T>C (p.Tyr378=) rs77570029 0.00211
NM_001044385.3(TMEM237):c.194A>G (p.Asn65Ser) rs141817764 0.00211
NM_001044385.3(TMEM237):c.396-14C>T rs74411816 0.00210
NM_001044385.3(TMEM237):c.348G>A (p.Ala116=) rs191125006 0.00163
NM_001044385.3(TMEM237):c.1065C>G (p.Leu355=) rs149240122 0.00111
NM_001044385.3(TMEM237):c.738G>A (p.Val246=) rs199947989 0.00006
NM_001044385.3(TMEM237):c.74+15C>T rs375401635 0.00006
NM_001044385.3(TMEM237):c.1024A>G (p.Asn342Asp) rs372686071 0.00004
NM_001044385.3(TMEM237):c.297A>G (p.Gln99=) rs767711440 0.00004
NM_001044385.3(TMEM237):c.136+1G>T rs778823927 0.00001
NM_001044385.3(TMEM237):c.1207G>T (p.Glu403Ter)
NM_001044385.3(TMEM237):c.550del (p.Ser184fs)
NM_001044385.3(TMEM237):c.596C>T (p.Thr199Ile)
NM_001044385.3(TMEM237):c.673_675delinsAT (p.Phe225fs)
NM_001044385.3(TMEM237):c.75-6T>C rs886038403
NM_001044385.3(TMEM237):c.870-13_870-12del rs555284377

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