Varaico: Literature-Extracted Genetic Variants

Gene:FLCN
Variant:p.S496_V497insFs

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
3 papers
NM_144997.7
p.S496_V497insFs
c.1487_1490dup4
Surrounding Variants
1 paper
NM_144997.7
p.V497insFs
c.1490_1491ins4
1 paper
NM_144997.7
p.D498Y
c.1492G>T
2 papers
NM_144997.7
p.V497delFs
c.1489_1490delAC
1 paper
NM_144997.7
p.S496delFs
c.1488delA
3 papers
NM_144997.7
p.V497fs
c.1489_1490fs
3 papers
NM_144997.7
p.V499insFs
c.1495_1496insTC
1 paper
NM_144997.7
p.V499_V500ins10
c.1495_1499ins30
2 papers
NM_144997.7
p.S496F
c.1487C>T
1 paper
NM_144997.7
p.S496C
c.1487C>G
1 paper
NM_144997.7
p.V500G
c.1499T>G
1 paper
NM_144997.7
p.V500E
c.1499T>A
1 paper
NM_144997.7
p.D501Y
c.1501G>T
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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."