Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.C591Y

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.C591Y
c.1772G>A
Surrounding Variants
1 paper
NM_000535.7
p.I590delFs
c.1769delA
1 paper
NM_000535.7
p.I590_C591Fs
c.1770_1772delinsCFs
1 paper
NM_000535.7
p.C591insFs
c.1771_1772insA
2 papers
NM_000535.7
p.C591R
c.1771T>C
1 paper
NM_000535.7
p.C591*
c.1773T>A
1 paper
NM_000535.7
p.C591delFs
c.1772delC
1 paper
NM_000535.7
p.Q592_K593insT
c.1774_1778ins3
2 papers
NM_000535.7
p.I590S
c.1769T>G
8 papers
NM_000535.7
p.I590delFs
c.1768delT
2 papers
NM_000535.7
p.I590fs
c.1768_1769fs
1 paper
NM_000535.7
p.Q592H
c.1776A>T
3 papers
NM_000535.7
p.I590V
c.1768A>G
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