Varaico: Literature-Extracted Genetic Variants

Gene:TTC8
Variant:p.C23delFs

TTC8

150 papers

RefSeq Summary

This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learn...

Pfam Domains

TPR_8aa 218–246UCSCTetratricopeptide repeat
TPR_8aa 282–315UCSCTetratricopeptide repeat
TPR_16aa 391–454UCSCTetratricopeptide repeat

Gene Aliases

HGNC Name

tetratricopeptide repeat domain 8

HGNC Alias Symbols

BBS8; RP51

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
2 papers
NM_144596.4
p.C23delFs
c.69delC
Surrounding Variants
1 paper
NM_144596.4
p.C23fs
c.67_68fs
1 paper
NM_144596.4
p.A24T
c.70G>A
1 paper
NM_144596.4
p.L22F
c.64C>T
1 paper
NM_144596.4
p.K19N
c.57G>C
1 paper
NM_144596.4
p.F20_L22del3
c.58_65del9
2 papers
NM_144596.4
p.F15_R16insFs
c.45_46insA
1 paper
NM_144596.4
p.W12C
c.36G>C
1 paper
NM_144596.4
p.W12C
c.36G>T
1 paper
NM_144596.4
p.L8Q
c.23T>A
2 papers
NM_001288781.1
p.Q38_A39Splc
c.114+1G>A
1 paper
NM_144596.4
p.Q38_E39Splc
c.114+2T>C
1 paper
NM_144596.4
p.E4fs
c.10_11fs
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