Varaico: Literature-Extracted Genetic Variants

Gene:INF2
Variant:p.G19W

INF2

339 papers

RefSeq Summary

This gene represents a member of the formin family of proteins. It is considered a diaphanous formin due to the presence of a diaphanous inhibitory domain located at the N-terminus of the encoded prot...

Pfam Domains

Drf_GBDaa 6–152UCSCDiaphanous GTPase-binding Domain
Drf_FH3aa 158–337UCSCDiaphanous FH3 Domain
FH2aa 554–921UCSCFormin Homology 2 Domain
WH2aa 974–991UCSCWH2 motif

Gene Aliases

HGNC Name

inverted formin 2

HGNC Previous Symbols

C14orf151; C14orf173

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
1 paper
NM_022489.4
p.G19W
c.55G>T
Surrounding Variants
1 paper
NM_022489.4
p.G19R
c.55G>A
1 paper
NM_022489.4
p.G19R
c.55G>C
1 paper
NM_022489.4
p.G19E
c.56G>A
2 papers
NM_022489.4
p.G19A
c.56G>C
1 paper
NM_022489.4
p.G19V
c.56G>T
1 paper
NM_022489.4
p.L18Q
c.53T>A
1 paper
NM_022489.4
p.L18P
c.53T>C
1 paper
NM_022489.4
p.L18R
c.53T>G
1 paper
NM_022489.4
p.L18M
c.52C>A
1 paper
NM_022489.4
p.P20T
c.58C>A
2 papers
NM_022489.4
p.L18V
c.52C>G
1 paper
NM_022489.4
p.P20A
c.58C>G
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."