Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.G655delFs

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.G655delFs
c.1963_1964delCC
Surrounding Variants
1 paper
NM_000535.7
p.G655delFs
c.1964delC
1 paper
NM_000535.7
p.G655E
c.1964G>A
1 paper
NM_000535.7
p.A650_P654del5
c.1948_1961del15
1 paper
NM_000535.7
p.K651_G655del5
c.1951_1964del15
1 paper
NM_000535.7
p.G655R
c.1963G>A
1 paper
NM_000535.7
p.C653_G655delFs
c.1958_1965del8
1 paper
NM_000535.7
p.P654insFs
c.1961dupC
5 papers
NM_000535.7
p.N657fs
c.1969_1970fs
8 papers
NM_000535.7
p.P654L
c.1961C>T
1 paper
NM_000535.7
p.C653_P654insFs
c.1957_1960dup4
2 papers
NM_000535.7
p.N657H
c.1969A>C
1 paper
NM_000535.7
p.P654T
c.1960C>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."