ClinVar Miner

List of variants in gene TCN2 reported as likely benign for anemia (disease)

Included ClinVar conditions (281):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_000355.3(TCN2):c.-250C>T rs5753231
NM_000355.4(TCN2):c.*209G>C rs146450057
NM_000355.4(TCN2):c.*300T>G rs187942607
NM_000355.4(TCN2):c.*313dup rs397940476
NM_000355.4(TCN2):c.1056G>A (p.Gly352=) rs370869901
NM_000355.4(TCN2):c.1086C>G (p.Ala362=) rs553587653
NM_000355.4(TCN2):c.1150G>A (p.Val384Met) rs144166182
NM_000355.4(TCN2):c.1164G>A (p.Ala388=) rs147747593
NM_000355.4(TCN2):c.210C>T (p.Asp70=) rs148829072
NM_000355.4(TCN2):c.249C>T (p.Cys83=) rs151327362
NM_000355.4(TCN2):c.280G>A (p.Gly94Ser) rs11557600
NM_000355.4(TCN2):c.296A>C (p.Lys99Thr) rs150225103
NM_000355.4(TCN2):c.360G>A (p.Arg120=) rs115272037
NM_000355.4(TCN2):c.428-7C>T rs778810764
NM_000355.4(TCN2):c.428-8C>T rs1412501560
NM_000355.4(TCN2):c.490C>T (p.Leu164=) rs754253807
NM_000355.4(TCN2):c.500A>T (p.His167Leu) rs200303429
NM_000355.4(TCN2):c.501C>T (p.His167=) rs144652799
NM_000355.4(TCN2):c.509G>A (p.Arg170Gln) rs117353193
NM_000355.4(TCN2):c.522C>T (p.Ser174=) rs537115632
NM_000355.4(TCN2):c.523G>A (p.Val175Met) rs142791153
NM_000355.4(TCN2):c.547G>A (p.Val183Met) rs201925682
NM_000355.4(TCN2):c.554C>T (p.Pro185Leu) rs146009793
NM_000355.4(TCN2):c.623G>A (p.Arg208His) rs150472705
NM_000355.4(TCN2):c.65-6del rs748765421
NM_000355.4(TCN2):c.65-8T>C rs773798398
NM_000355.4(TCN2):c.784G>C (p.Glu262Gln) rs61743653
NM_000355.4(TCN2):c.810G>T (p.Ala270=) rs61748898
NM_000355.4(TCN2):c.877C>T (p.Leu293=) rs45624233
NM_000355.4(TCN2):c.882C>T (p.Pro294=) rs142689742
NM_000355.4(TCN2):c.903C>T (p.Tyr301=) rs146036025
NM_000355.4(TCN2):c.921A>C (p.Pro307=) rs138738105

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