ClinVar Miner

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

Included ClinVar conditions (956):
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Total variants: 23
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HGVS dbSNP
NC_000005.10:g.95514896G>A
NM_014639.3(TTC37):c.1632+1del rs1060499527
NM_014639.3(TTC37):c.1783C>G (p.Pro595Ala) rs751343448
NM_014639.3(TTC37):c.2251C>T (p.Gln751Ter) rs387907148
NM_014639.3(TTC37):c.2494G>T (p.Gly832Cys)
NM_014639.3(TTC37):c.2515+1G>C rs1060499528
NM_014639.3(TTC37):c.2578-7_2578-3del rs746874042
NM_014639.3(TTC37):c.2808G>A (p.Trp936Ter) rs534237033
NM_014639.3(TTC37):c.3124G>C (p.Ala1042Pro) rs146638227
NM_014639.3(TTC37):c.3272del (p.Ile1090_Leu1091insTer)
NM_014639.3(TTC37):c.3808C>G (p.Pro1270Ala) rs146627706
NM_014639.3(TTC37):c.3885G>T (p.Lys1295Asn) rs892221746
NM_014639.3(TTC37):c.409C>T (p.Arg137Ter) rs776321294
NM_014639.3(TTC37):c.4187A>G (p.Asn1396Ser) rs116690692
NM_014639.3(TTC37):c.4310G>T (p.Ser1437Ile) rs755895621
NM_014639.3(TTC37):c.439C>T (p.Gln147Ter) rs387907147
NM_014639.3(TTC37):c.4620+1G>C rs370373017
NM_014639.4(TTC37):c.2275C>T (p.Leu759Phe)
NM_014639.4(TTC37):c.3015-4del
NM_014639.4(TTC37):c.4070del (p.Pro1357fs)
NM_014639.4(TTC37):c.4175_4176dup (p.Val1393fs)
NM_014639.4(TTC37):c.772C>T (p.Gln258Ter)
TTC37, IVS28AS, G-A, -2

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