Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.P568S

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.P568S
c.1702C>T
Surrounding Variants
1 paper
NM_000535.7
p.Q567insFs
c.1700dupA
1 paper
NM_000535.7
p.Q567H
c.1701G>C
1 paper
NM_000535.7
p.P568insFs
c.1702dupC
1 paper
NM_000535.7
p.Q567*
c.1699C>T
1 paper
NM_000535.7
p.P566delFs
c.1698delA
1 paper
NM_000535.7
p.L565_P566delFs
c.1695_1698del4
2 papers
NM_000535.7
p.T569A
c.1705A>G
2 papers
NM_000535.7
p.T569insFs
c.1705_1706insT
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.T569I
c.1706C>T
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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."