ClinVar Miner

List of variants in gene TTC8 studied for abdominal and pelvic region disorder

Included ClinVar conditions (956):
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Gene type:
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Total variants: 35
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HGVS dbSNP
NM_144596.3(TTC8):c.1049+2_1049+4del rs587777807
NM_144596.3(TTC8):c.1051C>T (p.Arg351Trp) rs755412340
NM_144596.3(TTC8):c.265+1_265+2del
NM_144596.3(TTC8):c.284A>G (p.Lys95Arg) rs150880478
NM_144596.3(TTC8):c.489G>A (p.Thr163=) rs119103286
NM_144596.3(TTC8):c.589_594del (p.Glu197_Tyr198del) rs587777806
NM_144596.3(TTC8):c.624+1G>A rs587777808
NM_198309.3(TTC8):c.*238G>A rs1048190
NM_198309.3(TTC8):c.*247T>C rs886050879
NM_198309.3(TTC8):c.*472A>C rs59300815
NM_198309.3(TTC8):c.*83A>G rs147325843
NM_198309.3(TTC8):c.-25G>A rs7145692
NM_198309.3(TTC8):c.-38C>A rs886050876
NM_198309.3(TTC8):c.-44C>T rs571786285
NM_198309.3(TTC8):c.1094A>C (p.Gln365Pro) rs774216735
NM_198309.3(TTC8):c.1297C>T (p.Arg433Trp) rs140698625
NM_198309.3(TTC8):c.1352C>T (p.Ala451Val) rs139195149
NM_198309.3(TTC8):c.1371G>A (p.Pro457=) rs114064158
NM_198309.3(TTC8):c.1387A>G (p.Thr463Ala) rs376411291
NM_198309.3(TTC8):c.1402-12T>C rs79747892
NM_198309.3(TTC8):c.1433C>T (p.Ala478Val) rs199649536
NM_198309.3(TTC8):c.1461C>T (p.Asp487=) rs886050878
NM_198309.3(TTC8):c.245C>T (p.Thr82Met) rs886050877
NM_198309.3(TTC8):c.300-15T>A rs187484893
NM_198309.3(TTC8):c.327T>C (p.Ile109=) rs567203939
NM_198309.3(TTC8):c.331G>A (p.Gly111Ser)
NM_198309.3(TTC8):c.440G>C (p.Arg147Thr) rs754686957
NM_198309.3(TTC8):c.454G>C (p.Gly152Arg) rs753150258
NM_198309.3(TTC8):c.460G>A (p.Ala154Thr)
NM_198309.3(TTC8):c.498T>C (p.Asn166=) rs1555391010
NM_198309.3(TTC8):c.5G>A (p.Ser2Asn) rs199571677
NM_198309.3(TTC8):c.639G>A (p.Lys213=) rs141304350
NM_198309.3(TTC8):c.697G>A (p.Glu233Lys)
NM_198309.3(TTC8):c.769-11C>T rs768485587
NM_198309.3(TTC8):c.875A>G (p.Tyr292Cys) rs370111364

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