Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.L47fs

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.L47fs
c.139_140fs
Surrounding Variants
5 papers
NM_000535.7
p.L47L
c.139C>T
5 papers
NM_000535.7
p.L47V
c.139C>G
1 paper
NM_000535.7
p.S46delFs
c.138delA
1 paper
NM_000535.7
p.S34_S46del13
c.100_137del39
1 paper
NM_000535.7
p.S46R
c.138T>G
2 papers
NM_000535.7
p.S46S
c.138T>C
1 paper
NM_000535.7
p.S46R
c.138T>A
171 papers
NM_000535.7
p.S46I
c.137G>T
1 paper
NM_000535.7
p.L47fs
c.139_140fs
22 papers
NM_000535.7
p.S46N
c.137G>A
2 papers
NM_000535.7
p.L47L
c.141G>A
1 paper
NM_000535.7
p.N45_L47delins
c.133_141delinsTGTTTT
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."