ClinVar Miner

List of variants in gene LOC121853040, TCN2 studied for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_000355.3(TCN2):c.-181A>G rs2240433 0.64970
NM_000355.3(TCN2):c.-250C>T rs5753231 0.14215
NM_000355.3(TCN2):c.-244C>T rs143029449 0.00657
NM_000355.4(TCN2):c.64+11C>T rs141519384 0.00203
NM_000355.4(TCN2):c.-98T>G rs370882214 0.00150
NM_000355.4(TCN2):c.64+13C>T rs370228236 0.00006
NM_000355.4(TCN2):c.-34A>G rs199511962 0.00005
NM_000355.3(TCN2):c.-191G>A rs886057394 0.00004
NM_000355.3(TCN2):c.-240G>A rs16988823 0.00004
NM_000355.4(TCN2):c.49C>G (p.Leu17Val) rs759462885 0.00004
NM_000355.4(TCN2):c.10C>T (p.Leu4Phe) rs572942248 0.00002
NM_000355.4(TCN2):c.-67C>T rs1432247695 0.00001
NM_000355.3(TCN2):c.-181A>C rs2240433
NM_000355.3(TCN2):c.-215C>T rs79083159
NM_000355.4(TCN2):c.-153C>G rs886057395
NM_000355.4(TCN2):c.-6G>A rs771507572
NM_000355.4(TCN2):c.17C>A (p.Ala6Asp) rs2145528950
NM_000355.4(TCN2):c.18C>T (p.Ala6=)
NM_000355.4(TCN2):c.19T>C (p.Phe7Leu)
NM_000355.4(TCN2):c.21C>T (p.Phe7=)
NM_000355.4(TCN2):c.24C>G (p.Leu8=)
NM_000355.4(TCN2):c.27C>T (p.Phe9=)
NM_000355.4(TCN2):c.30T>A (p.Leu10=) rs2145528985
NM_000355.4(TCN2):c.31C>G (p.Leu11Val) rs2145528995
NM_000355.4(TCN2):c.32T>C (p.Leu11Pro)
NM_000355.4(TCN2):c.33G>A (p.Leu11=)
NM_000355.4(TCN2):c.38del (p.Val13fs)
NM_000355.4(TCN2):c.44G>A (p.Gly15Glu)
NM_000355.4(TCN2):c.46_47delinsTT (p.Ala16Phe) rs2145529052
NM_000355.4(TCN2):c.54T>C (p.Thr18=)
NM_000355.4(TCN2):c.57G>A (p.Glu19=)
NM_000355.4(TCN2):c.64+12G>A
NM_000355.4(TCN2):c.64+14C>T
NM_000355.4(TCN2):c.64+15T>C
NM_000355.4(TCN2):c.64+16C>G rs2145529135
NM_000355.4(TCN2):c.64+18A>G
NM_000355.4(TCN2):c.64+19T>A
NM_000355.4(TCN2):c.64+20C>T
NM_000355.4(TCN2):c.64+4A>T
NM_000355.4(TCN2):c.64+9C>T
NM_000355.4(TCN2):c.9C>G (p.His3Gln) rs1489889957

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