Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.R295W

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
9 papers
NM_000535.7
p.R295W
c.883C>T
Surrounding Variants
1 paper
NM_000535.7
p.R294delFs
c.882delC
1 paper
NM_000535.7
p.R294delFs
c.881_882delCC
1 paper
NM_000535.7
p.N293_R295Fs
c.878_883delinsTTCGFs
4 papers
NM_000535.7
p.R295Q
c.884G>A
2 papers
NM_000535.7
p.R295_P296insFs
c.885_886insT
3 papers
NM_000535.7
p.R294P
c.881G>C
4 papers
NM_000535.7
p.R294Q
c.881G>A
4 papers
NM_000535.7
p.R294W
c.880C>T
1 paper
NM_000535.7
p.P296S
c.886C>T
2 papers
NM_000535.7
p.R294G
c.880C>G
1 paper
NM_000535.7
p.R295insFs
c.885dupG
1 paper
NM_000535.7
p.R294R
c.880C>A
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