Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.I668V

PMS2

2,219 papers

RefSeq Summary

The protein encoded by this gene is a key component of the mismatch repair system that functions to correct DNA mismatches and small insertions and deletions that can occur during DNA replication and ...

Pfam Domains

HATPase_c_3aa 33–162UCSCHistidine kinase-, DNA gyrase B-, and HSP90-like ATPase
HATPase_c_3aa 33–162UCSCHistidine kinase-, DNA gyrase B-, and HSP90-like ATPase
DNA_mis_repairaa 114–228UCSCDNA mismatch repair protein, C-terminal domain
DNA_mis_repairaa 249–363UCSCDNA mismatch repair protein, C-terminal domain
MutL_Caa 544–687UCSCMutL C terminal dimerisation domain

Gene Aliases

HGNC Name

PMS1 homolog 2, mismatch repair system component

HGNC Previous Symbol

PMSL2

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
15 papers
NM_000535.7
p.I668V
c.2002A>G
Surrounding Variants
1 paper
NM_000535.7
p.I668T
c.2003T>C
1 paper
NM_000535.7
p.E667_I668delFs
c.2001_2002delTC
1 paper
NM_000535.7
p.E667insFs
c.2000dupA
1 paper
NM_000535.7
p.I668Fs
c.2004delinsCAFs
1 paper
NM_000535.7
p.I668delFs
c.2003delA
2 papers
NM_000535.7
p.E667*
c.1999G>T
6 papers
NM_000535.7
p.E667K
c.1999G>A
6 papers
NM_000535.7
p.S669fs
c.2005_2006fs
1 paper
NM_000535.7
p.E667fs
c.1999_2000fs
4 papers
NM_000535.7
p.K666delFs
c.1997_1998delTT
2 papers
NM_000535.7
p.S669I
c.2006G>T
1 paper
NM_000535.7
p.S669N
c.2006G>A
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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."