Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.T458P

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
1 paper
NM_000535.7
p.T458P
c.1372A>C
Surrounding Variants
1 paper
NM_000535.7
p.T458delFs
c.1373delG
2 papers
NM_000535.7
p.S457I
c.1370G>T
1 paper
NM_000535.7
p.S457delFs
c.1369delT
1 paper
NM_000535.7
p.S457G
c.1369A>G
1 paper
NM_000535.7
p.S456insFs
c.1368dupT
1 paper
NM_000535.7
p.S459fs
c.1375_1376fs
1 paper
NM_000535.7
p.S456delFs
c.1367delG
2 papers
NM_000535.7
p.S459L
c.1376C>T
16 papers
NM_000535.7
p.S459*
c.1376C>G
16 papers
NM_000535.7
p.S459*
c.1376C>A
1 paper
NM_000535.7
p.S459delFs
c.1375delA
2 papers
NM_000535.7
p.S456C
c.1367C>G
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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."