ClinVar Miner

List of variants in gene TRNT1 studied for anemia (disease)

Included ClinVar conditions (262):
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Total variants: 41
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HGVS dbSNP
NM_182916.3(TRNT1):c.1045T>G (p.Phe349Val)
NM_182916.3(TRNT1):c.1056+1G>A
NM_182916.3(TRNT1):c.1057-7C>G rs368078167
NM_182916.3(TRNT1):c.1066C>T (p.Pro356Ser)
NM_182916.3(TRNT1):c.1079C>T (p.Thr360Ile) rs776480350
NM_182916.3(TRNT1):c.107A>T (p.Glu36Val)
NM_182916.3(TRNT1):c.1081C>T (p.Arg361Cys)
NM_182916.3(TRNT1):c.1142_1143insATGT (p.Trp381Ter) rs606231291
NM_182916.3(TRNT1):c.1252dup (p.Ser418fs) rs876661298
NM_182916.3(TRNT1):c.1292T>C (p.Ile431Thr) rs150984011
NM_182916.3(TRNT1):c.1295_1297AGA[1] (p.Lys433del)
NM_182916.3(TRNT1):c.133C>T (p.Leu45=) rs75033443
NM_182916.3(TRNT1):c.148+3G>A
NM_182916.3(TRNT1):c.185C>G (p.Ala62Gly)
NM_182916.3(TRNT1):c.215G>C (p.Gly72Ala) rs1267775202
NM_182916.3(TRNT1):c.231T>C (p.Asp77=) rs114362638
NM_182916.3(TRNT1):c.233T>C (p.Ile78Thr) rs1553553306
NM_182916.3(TRNT1):c.259A>G (p.Thr87Ala)
NM_182916.3(TRNT1):c.27C>T (p.His9=) rs776254990
NM_182916.3(TRNT1):c.284C>T (p.Ser95Leu) rs1287896952
NM_182916.3(TRNT1):c.295C>T (p.Arg99Trp)
NM_182916.3(TRNT1):c.324_330del (p.His108fs)
NM_182916.3(TRNT1):c.368C>G (p.Thr123Ser)
NM_182916.3(TRNT1):c.444G>T (p.Ala148=) rs41399044
NM_182916.3(TRNT1):c.461C>T (p.Thr154Ile) rs606231290
NM_182916.3(TRNT1):c.463A>G (p.Ile155Val)
NM_182916.3(TRNT1):c.488A>T (p.Asp163Val)
NM_182916.3(TRNT1):c.493A>G (p.Thr165Ala)
NM_182916.3(TRNT1):c.497T>C (p.Leu166Ser) rs606231289
NM_182916.3(TRNT1):c.514G>A (p.Gly172Ser)
NM_182916.3(TRNT1):c.557A>T (p.His186Leu)
NM_182916.3(TRNT1):c.567G>T (p.Gln189His)
NM_182916.3(TRNT1):c.569G>T (p.Arg190Ile) rs606231287
NM_182916.3(TRNT1):c.667A>G (p.Ile223Val)
NM_182916.3(TRNT1):c.668T>C (p.Ile223Thr) rs370011798
NM_182916.3(TRNT1):c.68= (p.Pro23=) rs334773
NM_182916.3(TRNT1):c.736C>T (p.Leu246Phe)
NM_182916.3(TRNT1):c.810_811insAAACTT (p.Ala271_Asn272insLysLeu) rs527331900
NM_182916.3(TRNT1):c.811G>A (p.Ala271Thr) rs1553555777
NM_182916.3(TRNT1):c.865del (p.Ser289fs)
NM_182916.3(TRNT1):c.925T>G (p.Leu309Val)

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