Varaico: Literature-Extracted Genetic Variants

Gene:AIPL1
Variant:p.L153V

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
1 paper
NM_014336.5
p.L153V
c.457C>G
Surrounding Variants
1 paper
NM_014336.5
p.Q141_L154del0
c.422_460del39
1 paper
NM_014336.5
p.Q155*
c.463C>T
2 papers
NM_014336.5
p.I151F
c.451A>T
12 papers
NM_014336.5
p.Q155H
c.465G>T
10 papers
NM_014336.5
p.Q155H
c.465G>C
1 paper
NM_014336.5
p.Q155_V156Splc
c.465+1G>C
2 papers
NM_014336.5
p.Q155_V156Splc
c.465+1G>A
1 paper
NM_014336.5
p.Q141_L154del14
c.421_461del42
1 paper
NM_014336.5
p.V148A
c.443T>C
1 paper
NM_014336.5
p.L147P
c.440T>C
1 paper
NM_014336.5
p.L147L
c.439C>T
1 paper
NM_014336.5
p.Q145*
c.433C>T
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