Varaico: Literature-Extracted Genetic Variants

Gene:FLCN
Variant:p.A238T

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
2 papers
NM_144997.7
p.A238T
c.712G>A
Surrounding Variants
3 papers
NM_144997.7
p.A238V
c.713C>T
1 paper
NM_144997.7
p.A237A
c.711C>T
1 paper
NM_144997.7
p.A238A
c.714C>A
1 paper
NM_144997.7
p.A237T
c.709G>A
29 papers
NM_144997.7
p.R239C
c.715C>T
6 papers
NM_144997.7
p.G235_A238del4
c.703_713del12
1 paper
NM_144997.7
p.R239L
c.716G>T
9 papers
NM_144997.7
p.R239H
c.716G>A
1 paper
NM_144997.7
p.N236N
c.708C>T
1 paper
NM_144997.7
p.N236S
c.707A>G
1 paper
NM_144997.7
p.S240P
c.718T>C
1 paper
NM_144997.7
p.Q232_G235delFs
c.696_705del10
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