ClinVar Miner

List of variants in gene TCN2 reported as uncertain significance for anemia (disease)

Included ClinVar conditions (281):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 93
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HGVS dbSNP
NM_000355.4(TCN2):c.*173C>T
NM_000355.4(TCN2):c.*18C>T
NM_000355.4(TCN2):c.*283C>G
NM_000355.4(TCN2):c.*329G>A
NM_000355.4(TCN2):c.*37C>T
NM_000355.4(TCN2):c.*381T>G rs149713328
NM_000355.4(TCN2):c.*383C>T
NM_000355.4(TCN2):c.*405T>C
NM_000355.4(TCN2):c.*415T>G
NM_000355.4(TCN2):c.*520T>C
NM_000355.4(TCN2):c.*93G>C rs886057398
NM_000355.4(TCN2):c.-153C>G rs886057395
NM_000355.4(TCN2):c.-34A>G rs199511962
NM_000355.4(TCN2):c.-67C>T
NM_000355.4(TCN2):c.-6G>A
NM_000355.4(TCN2):c.-98T>G rs370882214
NM_000355.4(TCN2):c.1017C>G (p.Leu339=) rs35997415
NM_000355.4(TCN2):c.1022C>T (p.Pro341Leu)
NM_000355.4(TCN2):c.1043C>G (p.Ser348Cys)
NM_000355.4(TCN2):c.1052C>T (p.Ala351Val) rs951348375
NM_000355.4(TCN2):c.1058C>G (p.Ser353Cys) rs539987014
NM_000355.4(TCN2):c.1063G>A (p.Val355Met)
NM_000355.4(TCN2):c.1092G>A (p.Glu364=) rs886057397
NM_000355.4(TCN2):c.109C>T (p.His37Tyr) rs1326813642
NM_000355.4(TCN2):c.10C>T (p.Leu4Phe) rs572942248
NM_000355.4(TCN2):c.1109A>G (p.Tyr370Cys) rs1406364381
NM_000355.4(TCN2):c.1121CCT[1] (p.Ser375del)
NM_000355.4(TCN2):c.1139A>G (p.Tyr380Cys)
NM_000355.4(TCN2):c.1168G>A (p.Gly390Arg) rs367605153
NM_000355.4(TCN2):c.1195C>G (p.Arg399Gly) rs769817524
NM_000355.4(TCN2):c.1229C>G (p.Ala410Gly)
NM_000355.4(TCN2):c.1235A>G (p.Tyr412Cys) rs745363222
NM_000355.4(TCN2):c.1237A>G (p.Arg413Gly) rs148963479
NM_000355.4(TCN2):c.1246G>A (p.Asp416Asn) rs773473997
NM_000355.4(TCN2):c.138C>T (p.Ser46=) rs143250551
NM_000355.4(TCN2):c.139C>A (p.Leu47Met)
NM_000355.4(TCN2):c.154C>T (p.Pro52Ser) rs1555894597
NM_000355.4(TCN2):c.164A>G (p.Tyr55Cys) rs201701227
NM_000355.4(TCN2):c.175C>T (p.Arg59Cys) rs757905563
NM_000355.4(TCN2):c.184A>G (p.Ser62Gly)
NM_000355.4(TCN2):c.197G>C (p.Gly66Ala)
NM_000355.4(TCN2):c.242A>C (p.Gln81Pro)
NM_000355.4(TCN2):c.280G>C (p.Gly94Arg)
NM_000355.4(TCN2):c.296A>C (p.Lys99Thr) rs150225103
NM_000355.4(TCN2):c.299C>T (p.Pro100Leu) rs752901101
NM_000355.4(TCN2):c.323A>T (p.Tyr108Phe) rs781309237
NM_000355.4(TCN2):c.331G>A (p.Ala111Thr)
NM_000355.4(TCN2):c.353T>C (p.Phe118Ser) rs199728304
NM_000355.4(TCN2):c.362G>A (p.Gly121Asp) rs1602045889
NM_000355.4(TCN2):c.408G>C (p.Glu136Asp) rs886057396
NM_000355.4(TCN2):c.409G>A (p.Asp137Asn) rs775586639
NM_000355.4(TCN2):c.425T>C (p.Ile142Thr)
NM_000355.4(TCN2):c.428-4T>C rs201408393
NM_000355.4(TCN2):c.430C>T (p.His144Tyr)
NM_000355.4(TCN2):c.459C>T (p.Ser153=) rs201344377
NM_000355.4(TCN2):c.522C>T (p.Ser174=) rs537115632
NM_000355.4(TCN2):c.529G>A (p.Asp177Asn)
NM_000355.4(TCN2):c.559C>T (p.His187Tyr)
NM_000355.4(TCN2):c.562C>T (p.Gln188Ter) rs1456983114
NM_000355.4(TCN2):c.566G>A (p.Gly189Asp) rs777945731
NM_000355.4(TCN2):c.572A>G (p.His191Arg) rs151172486
NM_000355.4(TCN2):c.581-4C>T
NM_000355.4(TCN2):c.581-8A>G rs7290898
NM_000355.4(TCN2):c.638C>T (p.Pro213Leu)
NM_000355.4(TCN2):c.64+11C>T rs141519384
NM_000355.4(TCN2):c.644G>A (p.Arg215Gln) rs760721315
NM_000355.4(TCN2):c.65-6T>A rs1602043415
NM_000355.4(TCN2):c.655A>G (p.Ile219Val)
NM_000355.4(TCN2):c.70C>A (p.Pro24Thr) rs755866662
NM_000355.4(TCN2):c.70C>T (p.Pro24Ser) rs755866662
NM_000355.4(TCN2):c.737C>T (p.Thr246Ile) rs147738100
NM_000355.4(TCN2):c.787C>G (p.Leu263Val)
NM_000355.4(TCN2):c.809C>T (p.Ala270Val) rs201392026
NM_000355.4(TCN2):c.810G>A (p.Ala270=) rs61748898
NM_000355.4(TCN2):c.810G>T (p.Ala270=) rs61748898
NM_000355.4(TCN2):c.843A>T (p.Gly281=) rs979235252
NM_000355.4(TCN2):c.855T>A (p.Asn285Lys)
NM_000355.4(TCN2):c.857C>T (p.Ala286Val)
NM_000355.4(TCN2):c.859C>T (p.Leu287Phe)
NM_000355.4(TCN2):c.868T>G (p.Ser290Ala)
NM_000355.4(TCN2):c.882C>T (p.Pro294=) rs142689742
NM_000355.4(TCN2):c.883G>A (p.Val295Ile)
NM_000355.4(TCN2):c.899C>T (p.Thr300Ile)
NM_000355.4(TCN2):c.903C>T (p.Tyr301=) rs146036025
NM_000355.4(TCN2):c.905T>C (p.Ile302Thr)
NM_000355.4(TCN2):c.921A>C (p.Pro307=) rs138738105
NM_000355.4(TCN2):c.926G>A (p.Cys309Tyr)
NM_000355.4(TCN2):c.937C>G (p.Arg313Gly)
NM_000355.4(TCN2):c.988A>G (p.Ile330Val)
NM_000355.4(TCN2):c.9C>G (p.His3Gln)
NM_001184726.1(TCN2):c.-181A>C rs2240433
NM_001184726.1(TCN2):c.-191G>A rs886057394
NM_001184726.1(TCN2):c.-240G>A

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