Varaico: Literature-Extracted Genetic Variants

Gene:AIPL1
Variant:p.C239R

AIPL1

337 papers

RefSeq Summary

Leber congenital amaurosis (LCA) is the most severe inherited retinopathy with the earliest age of onset and accounts for at least 5% of all inherited retinal diseases. Affected individuals are diagno...

Pfam Domains

PPIase_AIPaa 12–155UCSCAH receptor-interacting protein, N-terminal FKBP-type PPIase

Gene Aliases

HGNC Name

AIP like 1 HSP90 co-chaperone

HGNC Previous Symbol

LCA4

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
22 papers
NM_014336.5
p.C239R
c.715T>C
Surrounding Variants
2 papers
NM_014336.5
p.C239F
c.716G>T
1 paper
NM_014336.5
p.Q238H
c.714G>C
1 paper
NM_014336.5
p.C237W
c.711C>G
1 paper
NM_014336.5
p.C237*
c.711C>A
1 paper
NM_014336.5
p.Y236_C237insFs
c.708_709dupCT
1 paper
NM_014336.5
p.L232_L241delFs
c.694_722del29
1 paper
NM_014336.5
p.N235del1
c.703_705delGTT
2 papers
NM_014336.5
p.L241del1
c.721_722delCAG
2 papers
NM_014336.5
p.L241_K242del1
c.723_725delTTC
2 papers
NM_014336.5
p.E245*
c.733G>T
1 paper
NM_014336.5
p.E245K
c.733G>A
1 paper
NM_014336.5
p.E245insFs
c.733dupG
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