ClinVar Miner

List of variants in gene TRIOBP reported as uncertain significance for auditory system disease

Included ClinVar conditions (549):
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Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_001039141.3(TRIOBP):c.1195C>G (p.Arg399Gly)
NM_001039141.3(TRIOBP):c.1283C>G (p.Pro428Arg) rs372134073
NM_001039141.3(TRIOBP):c.154G>A (p.Asp52Asn) rs147691840
NM_001039141.3(TRIOBP):c.2018G>A (p.Arg673Lys) rs370666072
NM_001039141.3(TRIOBP):c.2061_2132del (p.Ser688_Pro711del) rs1569041188
NM_001039141.3(TRIOBP):c.2064C>A (p.Ser688Arg) rs1555896093
NM_001039141.3(TRIOBP):c.2149C>G (p.Gln717Glu) rs186620158
NM_001039141.3(TRIOBP):c.3214C>G (p.Arg1072Gly)
NM_001039141.3(TRIOBP):c.3692G>A (p.Arg1231His)
NM_001039141.3(TRIOBP):c.3910C>T (p.Arg1304Cys)
NM_001039141.3(TRIOBP):c.4483G>T (p.Glu1495Ter)
NM_001039141.3(TRIOBP):c.4792C>G (p.Pro1598Ala) rs201730395
NM_001039141.3(TRIOBP):c.536G>C (p.Arg179Pro) rs773013563
NM_001039141.3(TRIOBP):c.5476A>C (p.Thr1826Pro)
NM_001039141.3(TRIOBP):c.5705A>C (p.Lys1902Thr) rs138804394
NM_001039141.3(TRIOBP):c.6049G>C (p.Asp2017His)
NM_001039141.3(TRIOBP):c.6328G>A (p.Ala2110Thr)
NM_001039141.3(TRIOBP):c.6362C>T (p.Ser2121Leu) rs201724032
NM_001039141.3(TRIOBP):c.6515G>A (p.Arg2172Gln) rs200528850
NM_001039141.3(TRIOBP):c.6548G>A (p.Gly2183Asp) rs780554525
NM_001039141.3(TRIOBP):c.6632A>T (p.Gln2211Leu)
NM_001039141.3(TRIOBP):c.6803G>A (p.Gly2268Asp) rs200411253
NM_001039141.3(TRIOBP):c.6860G>A (p.Arg2287His) rs370737996
NM_001039141.3(TRIOBP):c.964G>T (p.Ala322Ser)

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