Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.A636P

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
12 papers
NM_000535.7
p.A636P
c.1906G>C
Surrounding Variants
1 paper
NM_000535.7
p.E635insFs
c.1904dupA
2 papers
NM_000535.7
p.E635_A636Fs
c.1905_1906delinsTFs
1 paper
NM_000535.7
p.A636fs
c.1906_1907fs
1 paper
NM_000535.7
p.A636V
c.1907C>T
2 papers
NM_000535.7
p.E635fs
c.1903_1904fs
1 paper
NM_000535.7
p.E635V
c.1904A>T
1 paper
NM_000535.7
p.E635G
c.1904A>G
1 paper
NM_000535.7
p.A636delFs
c.1907delG
2 papers
NM_000535.7
p.E635*
c.1903G>T
1 paper
NM_000535.7
p.H634delFs
c.1902delA
1 paper
NM_000535.7
p.H634delFs
c.1901_1902delAT
1 paper
NM_000535.7
p.Q631_H634del4
c.1891_1901del12
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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."