ClinVar Miner

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

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP
NM_000355.3(TCN2):c.*209G>C rs146450057
NM_000355.3(TCN2):c.*300T>G rs187942607
NM_000355.3(TCN2):c.*381T>G rs149713328
NM_000355.3(TCN2):c.*382C>T rs56076607
NM_000355.3(TCN2):c.*93G>C rs886057398
NM_000355.3(TCN2):c.-153C>G rs886057395
NM_000355.3(TCN2):c.-181A>C rs2240433
NM_000355.3(TCN2):c.-191G>A rs886057394
NM_000355.3(TCN2):c.-244C>T rs143029449
NM_000355.3(TCN2):c.-34A>G rs199511962
NM_000355.3(TCN2):c.-98T>G rs370882214
NM_000355.3(TCN2):c.1017C>G (p.Leu339=) rs35997415
NM_000355.3(TCN2):c.1058C>G (p.Ser353Cys) rs539987014
NM_000355.3(TCN2):c.1092G>A (p.Glu364=) rs886057397
NM_000355.3(TCN2):c.1168G>A (p.Gly390Arg)
NM_000355.3(TCN2):c.1195C>G (p.Arg399Gly)
NM_000355.3(TCN2):c.1235A>G (p.Tyr412Cys)
NM_000355.3(TCN2):c.1237A>G (p.Arg413Gly) rs148963479
NM_000355.3(TCN2):c.1246G>A (p.Asp416Asn)
NM_000355.3(TCN2):c.138C>T (p.Ser46=) rs143250551
NM_000355.3(TCN2):c.154C>T (p.Pro52Ser) rs1555894597
NM_000355.3(TCN2):c.164A>G (p.Tyr55Cys)
NM_000355.3(TCN2):c.175C>T (p.Arg59Cys) rs757905563
NM_000355.3(TCN2):c.265T>C (p.Phe89Leu) rs35915865
NM_000355.3(TCN2):c.299C>T (p.Pro100Leu)
NM_000355.3(TCN2):c.323A>T (p.Tyr108Phe)
NM_000355.3(TCN2):c.353T>C (p.Phe118Ser) rs199728304
NM_000355.3(TCN2):c.408G>C (p.Glu136Asp) rs886057396
NM_000355.3(TCN2):c.409G>A (p.Asp137Asn) rs775586639
NM_000355.3(TCN2):c.428-4T>C rs201408393
NM_000355.3(TCN2):c.459C>T (p.Ser153=) rs201344377
NM_000355.3(TCN2):c.501C>T (p.His167=) rs144652799
NM_000355.3(TCN2):c.509G>A (p.Arg170Gln) rs117353193
NM_000355.3(TCN2):c.554C>T (p.Pro185Leu) rs146009793
NM_000355.3(TCN2):c.562C>T (p.Gln188Ter) rs1456983114
NM_000355.3(TCN2):c.64+11C>T rs141519384
NM_000355.3(TCN2):c.644G>A (p.Arg215Gln) rs760721315
NM_000355.3(TCN2):c.70C>T (p.Pro24Ser) rs755866662
NM_000355.3(TCN2):c.737C>T (p.Thr246Ile)
NM_000355.3(TCN2):c.809C>T (p.Ala270Val) rs201392026
NM_000355.3(TCN2):c.810G>T (p.Ala270=) rs61748898
NM_000355.3(TCN2):c.840T>C (p.Asp280=) rs79999752
NM_000355.3(TCN2):c.877C>T (p.Leu293=) rs45624233
NM_000355.3(TCN2):c.903C>T (p.Tyr301=) rs146036025
NM_000355.3(TCN2):c.921A>C (p.Pro307=) rs138738105
NM_000355.3(TCN2):c.941-13C>T rs192009509

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