Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.M600T

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
2 papers
NM_000535.7
p.M600T
c.1799T>C
Surrounding Variants
3 papers
NM_000535.7
p.M600K
c.1799T>A
1 paper
NM_000535.7
p.D599delFs
c.1796_1797delGT
1 paper
NM_000535.7
p.Q598_D599delFs
c.1792_1796del5
1 paper
NM_000535.7
p.D599delFs
c.1796delT
2 papers
NM_000535.7
p.S601*
c.1802C>G
1 paper
NM_000535.7
p.S601*
c.1802C>A
1 paper
NM_000535.7
p.Q598insFs
c.1794dupG
1 paper
NM_000535.7
p.D599Y
c.1795G>T
1 paper
NM_000535.7
p.D599N
c.1795G>A
1 paper
NM_000535.7
p.T597_Q598del2
c.1789_1793del6
1 paper
NM_000535.7
p.S601insFs
c.1803dupA
2 papers
NM_000535.7
p.Q598delFs
c.1793delT
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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."