Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.M1Fs

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
2 papers
NM_000535.7
p.M1Fs
c.3delinsAGFs
Surrounding Variants
4 papers
NM_000535.7
p.M1I
c.3G>T
5 papers
NM_000535.7
p.M1insFs
c.2_3insT
1 paper
NM_000535.7
p.M1_E2insFs
c.3_4insTT
3 papers
NM_000535.7
p.M1I
c.3G>C
8 papers
NM_000535.7
p.M1I
c.3G>A
1 paper
NM_000535.7
p.M1insFs
c.2_3ins4
1 paper
NM_000535.7
p.M1delins
c.1delinsACAC
3 papers
NM_000535.7
p.M1insFs
c.1dupA
5 papers
NM_000535.7
p.M1R
c.2T>G
1 paper
NM_000535.7
p.M1Fs
c.2delinsACGFs
16 papers
NM_000535.7
p.M1T
c.2T>C
26 papers
NM_000535.7
p.M1K
c.2T>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."