ClinVar Miner

List of variants in gene TTC37 studied for abdominal and pelvic region disorder

Included ClinVar conditions (891):
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Total variants: 14
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HGVS dbSNP
NG_023414.1:g.43590_43594del rs746874042
NM_014639.3(TTC37):c.1632+1delG rs1060499527
NM_014639.3(TTC37):c.1783C>G (p.Pro595Ala)
NM_014639.3(TTC37):c.2251C>T (p.Gln751Ter) rs387907148
NM_014639.3(TTC37):c.2515+1G>C rs1060499528
NM_014639.3(TTC37):c.2808G>A (p.Trp936Ter) rs534237033
NM_014639.3(TTC37):c.3124G>C (p.Ala1042Pro)
NM_014639.3(TTC37):c.3808C>G (p.Pro1270Ala) rs146627706
NM_014639.3(TTC37):c.3885G>T (p.Lys1295Asn)
NM_014639.3(TTC37):c.409C>T (p.Arg137Ter)
NM_014639.3(TTC37):c.4310G>T (p.Ser1437Ile)
NM_014639.3(TTC37):c.439C>T (p.Gln147Ter) rs387907147
NM_014639.3(TTC37):c.4620+1G>C rs370373017
TTC37, IVS28AS, G-A, -2

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