Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.H845Q

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.H845Q
c.2535T>A
Surrounding Variants
1 paper
NM_000535.7
p.H845fs
c.2533_2534fs
1 paper
NM_000535.7
p.H845Q
c.2535T>G
1 paper
NM_000535.7
p.G846*
c.2536G>T
1 paper
NM_000535.7
p.H845insFs
c.2535dupT
1 paper
NM_000535.7
p.P840_H845del6
c.2518_2534del18
1 paper
NM_000535.7
p.H845R
c.2534A>G
1 paper
NM_000535.7
p.P844insFs
c.2532dupC
2 papers
NM_000535.7
p.H845delFs
c.2533delG
1 paper
NM_000535.7
p.H845fs
c.2533_2534fs
1 paper
NM_000535.7
p.G846A
c.2537G>C
1 paper
NM_000535.7
p.P844_H845delins
c.2532_2533delinsCT
6 papers
NM_000535.7
p.H845D
c.2533C>G
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