ClinVar Miner

List of variants in gene TSTD2 reported as uncertain significance by Ambry Genetics

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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_139246.5(TSTD2):c.1516C>A (p.Pro506Thr) rs140224495 0.00148
NM_139246.5(TSTD2):c.1519G>A (p.Asp507Asn) rs147770827 0.00019
NM_139246.5(TSTD2):c.807C>A (p.Ser269Arg) rs760448403 0.00007
NM_139246.5(TSTD2):c.629A>G (p.Asn210Ser) rs779224859 0.00006
NM_139246.5(TSTD2):c.1078C>T (p.Arg360Cys) rs148394086 0.00005
NM_139246.5(TSTD2):c.22G>A (p.Asp8Asn) rs200931295 0.00005
NM_139246.5(TSTD2):c.278A>G (p.His93Arg) rs775584995 0.00004
NM_139246.5(TSTD2):c.1088G>A (p.Arg363Gln) rs554393071 0.00003
NM_139246.5(TSTD2):c.1547T>C (p.Met516Thr) rs772250062 0.00003
NM_139246.5(TSTD2):c.761A>G (p.Glu254Gly) rs139054763 0.00003
NM_139246.5(TSTD2):c.767G>A (p.Arg256His) rs756280716 0.00003
NM_139246.5(TSTD2):c.367A>G (p.Lys123Glu) rs555917350 0.00002
NM_139246.5(TSTD2):c.1273C>T (p.Arg425Cys) rs759843680 0.00001
NM_139246.5(TSTD2):c.1459C>T (p.Arg487Cys) rs773614212 0.00001
NM_139246.5(TSTD2):c.275T>C (p.Ile92Thr) rs761083665 0.00001
NM_139246.5(TSTD2):c.299A>G (p.His100Arg) rs575567532 0.00001
NM_139246.5(TSTD2):c.664C>T (p.Leu222Phe) rs200295410 0.00001
NM_139246.5(TSTD2):c.956G>A (p.Gly319Glu) rs773285444 0.00001
NM_139246.5(TSTD2):c.959G>A (p.Arg320Gln) rs747917068 0.00001
NM_139246.5(TSTD2):c.1010G>A (p.Ser337Asn) rs2490005408
NM_139246.5(TSTD2):c.1022A>G (p.Lys341Arg)
NM_139246.5(TSTD2):c.1038C>G (p.Phe346Leu)
NM_139246.5(TSTD2):c.1049G>C (p.Arg350Thr) rs139574256
NM_139246.5(TSTD2):c.1079G>A (p.Arg360His) rs753069573
NM_139246.5(TSTD2):c.112A>C (p.Lys38Gln)
NM_139246.5(TSTD2):c.1148G>T (p.Gly383Val)
NM_139246.5(TSTD2):c.1163T>G (p.Leu388Arg)
NM_139246.5(TSTD2):c.1246G>A (p.Val416Met) rs2490003655
NM_139246.5(TSTD2):c.1298C>G (p.Ser433Cys) rs150422288
NM_139246.5(TSTD2):c.13A>G (p.Thr5Ala)
NM_139246.5(TSTD2):c.1406G>A (p.Gly469Asp)
NM_139246.5(TSTD2):c.1469G>T (p.Arg490Met) rs149901043
NM_139246.5(TSTD2):c.1471G>A (p.Glu491Lys) rs1239083382
NM_139246.5(TSTD2):c.1472A>C (p.Glu491Ala)
NM_139246.5(TSTD2):c.22G>C (p.Asp8His)
NM_139246.5(TSTD2):c.262G>A (p.Asp88Asn)
NM_139246.5(TSTD2):c.274A>C (p.Ile92Leu)
NM_139246.5(TSTD2):c.311T>G (p.Ile104Ser)
NM_139246.5(TSTD2):c.364T>A (p.Ser122Thr) rs774683481
NM_139246.5(TSTD2):c.394A>G (p.Asn132Asp)
NM_139246.5(TSTD2):c.40G>C (p.Glu14Gln) rs2490032603
NM_139246.5(TSTD2):c.430G>A (p.Val144Met)
NM_139246.5(TSTD2):c.569C>T (p.Thr190Ile)
NM_139246.5(TSTD2):c.5C>T (p.Pro2Leu) rs2490032662
NM_139246.5(TSTD2):c.608G>A (p.Arg203Gln)
NM_139246.5(TSTD2):c.641G>T (p.Gly214Val) rs751553437
NM_139246.5(TSTD2):c.647G>A (p.Ser216Asn)
NM_139246.5(TSTD2):c.662G>C (p.Arg221Thr)
NM_139246.5(TSTD2):c.712T>G (p.Cys238Gly)
NM_139246.5(TSTD2):c.737A>G (p.Lys246Arg)
NM_139246.5(TSTD2):c.760G>A (p.Glu254Lys)
NM_139246.5(TSTD2):c.773G>T (p.Gly258Val) rs367969850
NM_139246.5(TSTD2):c.790G>T (p.Val264Leu) rs750388352
NM_139246.5(TSTD2):c.842A>G (p.His281Arg)
NM_139246.5(TSTD2):c.980C>T (p.Pro327Leu)

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