Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.R563delFs

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.R563delFs
c.1688_1689delTC
Surrounding Variants
1 paper
NM_000535.7
p.R563insFs
c.1689dupA
1 paper
NM_000535.7
p.V564I
c.1690G>A
1 paper
NM_000535.7
p.L565V
c.1693T>G
3 papers
NM_000535.7
p.R563R
c.1689A>G
4 papers
NM_000535.7
p.R563delins
c.1688_1689delinsAG
1 paper
NM_000535.7
p.V564_L565delFs
c.1690_1693del4
1 paper
NM_000535.7
p.R563_L565delFs
c.1687_1693del7
38 papers
NM_000535.7
p.R563L
c.1688G>T
1 paper
NM_000535.7
p.R563insFs
c.1687dupC
18 papers
NM_000535.7
p.R563Q
c.1688G>A
1 paper
NM_000535.7
p.V564_L565delFs
c.1692_1693delAA
41 papers
NM_000535.7
p.R563*
c.1687C>T
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