Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.N293delFs

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.N293delFs
c.878_879delGT
Surrounding Variants
4 papers
NM_000535.7
p.R294W
c.880C>T
2 papers
NM_000535.7
p.R294G
c.880C>G
1 paper
NM_000535.7
p.R294R
c.880C>A
1 paper
NM_000535.7
p.N293_R294Fs
c.878_880delinsTFs
3 papers
NM_000535.7
p.R294P
c.881G>C
4 papers
NM_000535.7
p.R294Q
c.881G>A
1 paper
NM_000535.7
p.N293K
c.879C>G
1 paper
NM_000535.7
p.N293insFs
c.878dupA
2 papers
NM_000535.7
p.N293S
c.878A>G
9 papers
NM_000535.7
p.R295W
c.883C>T
1 paper
NM_000535.7
p.R294delFs
c.882delC
1 paper
NM_000535.7
p.R294delFs
c.881_882delCC
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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."