Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.R153fs

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.R153fs
c.457_458fs
Surrounding Variants
3 papers
NM_000535.7
p.P152insFs
c.455dupC
1 paper
NM_000535.7
p.P152delFs
c.454delG
1 paper
NM_000535.7
p.R151_R153Fs
c.452_457delinsCCCCGFs
1 paper
NM_000535.7
p.R153delFs
c.457delT
1 paper
NM_000535.7
p.P152P
c.456C>G
1 paper
NM_000535.7
p.G154_T155insG
c.460_464ins3
1 paper
NM_000535.7
p.G154R
c.460G>C
3 papers
NM_000535.7
p.G154R
c.460G>A
1 paper
NM_000535.7
p.R153delFs
c.459delT
2 papers
NM_000535.7
p.P152_R153delFs
c.456_459del4
1 paper
NM_000535.7
p.P150_R153del4
c.448_458del12
2 papers
NM_000535.7
p.G154E
c.461G>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."