Varaico: Literature-Extracted Genetic Variants

Gene:FLCN
Variant:p.Q458fs

FLCN

815 papers

RefSeq Summary

This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal t...

Pfam Domains

Folliculinaa 104–265UCSCVesicle coat protein involved in Golgi to plasma membrane transport
Folliculin_Caa 344–566UCSCFolliculin C-terminal domain

Gene Aliases

HGNC Name

folliculin

HGNC Alias Symbols

BHD; MGC17998; MGC23445; DENND8B

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
1 paper
NM_144997.7
p.Q458fs
c.1372_1373fs
Surrounding Variants
1 paper
NM_144997.7
p.S459A
c.1375T>G
2 papers
NM_144997.7
p.Q458R
c.1373A>G
2 papers
NM_144997.7
p.Q458insFs
c.1372dupC
1 paper
NM_144997.7
p.Q458fs
c.1372_1373fs
1 paper
NM_144997.7
p.S459F
c.1376C>T
1 paper
NM_144997.7
p.Q458*
c.1372C>T
4 papers
NM_144997.7
p.L460fs
c.1378_1379fs
1 paper
NM_144997.7
p.L460L
c.1380C>T
2 papers
NM_144997.7
p.L460fs
c.1378_1379fs
1 paper
NM_144997.7
p.S461fs
c.1381_1382fs
1 paper
NM_144997.7
p.D456G
c.1367A>G
15 papers
NM_144997.7
p.L460delFs
c.1379_1380delGA
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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."