Varaico: Literature-Extracted Genetic Variants

Gene:TTC8
Variant:p.G121D

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
1 paper
NM_144596.4
p.G121D
c.362G>A
Surrounding Variants
1 paper
NM_144596.4
p.T120A
c.358A>G
1 paper
NM_144596.4
p.I119insFs
c.355_356ins13
5 papers
NM_144596.4
p.I119insFs
c.355_356ins16
1 paper
NM_144596.4
p.G116V
c.347G>T
1 paper
NM_144596.4
p.Q128*
c.382C>T
2 papers
NM_001288781.1
p.S119insFs
c.355_356ins16
1 paper
NM_198309.3
p.S119insFs
c.355_356ins13
1 paper
NM_001288781.1
p.T103_Q104insFs
c.309_310insTA
1 paper
NM_001288781.1
p.T103fs
c.307_308fs
1 paper
NM_144596.4
p.P111P
c.333A>G
1 paper
NM_144596.4
p.T134delFs
c.402delT
2 papers
NM_144596.4
p.M135I
c.405G>A
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."