Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.N596S

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
6 papers
NM_000535.7
p.N596S
c.1787A>G
Surrounding Variants
1 paper
NM_000535.7
p.N596insFs
c.1787dupA
1 paper
NM_000535.7
p.N596fs
c.1786_1787fs
39 papers
NM_000535.7
p.T597S
c.1789A>T
1 paper
NM_000535.7
p.T597A
c.1789A>G
1 paper
NM_000535.7
p.V595insFs
c.1784dupT
1 paper
NM_000535.7
p.T597_Q598ins4
c.1789_1793ins12
1 paper
NM_000535.7
p.V595_N596insFs
c.1785_1786ins14
3 papers
NM_000535.7
p.V595delFs
c.1784delA
1 paper
NM_000535.7
p.V595delFs
c.1783_1784delAC
1 paper
NM_000535.7
p.K593_L594delFs
c.1779_1782del4
1 paper
NM_000535.7
p.V595G
c.1784T>G
34 papers
NM_000535.7
p.T597S
c.1790C>G
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