Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.R563_L565delFs

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.R563_L565delFs
c.1687_1693del7
Surrounding Variants
1 paper
NM_000535.7
p.V564_L565delFs
c.1690_1693del4
1 paper
NM_000535.7
p.L565V
c.1693T>G
1 paper
NM_000535.7
p.V564_L565delFs
c.1692_1693delAA
1 paper
NM_000535.7
p.P566S
c.1696C>T
1 paper
NM_000535.7
p.R563delFs
c.1688_1689delTC
1 paper
NM_000535.7
p.P566L
c.1697C>T
1 paper
NM_000535.7
p.P566R
c.1697C>G
1 paper
NM_000535.7
p.P566P
c.1698T>A
1 paper
NM_000535.7
p.P566delFs
c.1697delG
1 paper
NM_000535.7
p.P566delFs
c.1696_1697delGG
1 paper
NM_000535.7
p.R563insFs
c.1689dupA
1 paper
NM_000535.7
p.V564I
c.1690G>A
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