Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.T37delFs

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.T37delFs
c.111delA
Surrounding Variants
1 paper
NM_000535.7
p.A38_V39insG
c.112_116ins3
1 paper
NM_000535.7
p.A38_V39ins4
c.112_116ins12
2 papers
NM_000535.7
p.A38T
c.112G>A
1 paper
NM_000535.7
p.T37T
c.111T>C
1 paper
NM_000535.7
p.T37delFs
c.110delG
1 paper
NM_000535.7
p.V32_T37delFs
c.94_110del17
9 papers
NM_000535.7
p.A38V
c.113C>T
1 paper
NM_000535.7
p.S36_A38ins1
c.108_113dup6
2 papers
NM_000535.7
p.A38A
c.114G>A
1 paper
NM_000535.7
p.L35_A38delFs
c.103_113del11
1 paper
NM_000535.7
p.T37I
c.110C>T
1 paper
NM_000535.7
p.V39L
c.115G>T
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