Varaico: Literature-Extracted Genetic Variants

Gene:PMS2
Variant:p.*863G

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.*863G
c.2587T>G
Surrounding Variants
1 paper
NM_000535.7
p.I853_N862delFs
c.2558_2586del29
1 paper
NM_000535.7
p.N862insFs
c.2585dupA
1 paper
NM_000535.7
p.*863insFs
c.2588dupG
1 paper
NM_000535.7
p.N862insFs
c.2585_2586insC
6 papers
NM_000535.7
p.N862_*863del2
c.2584_2588del6
1 paper
NM_000535.7
p.Q861Q
c.2583G>A
1 paper
NM_000535.7
p.Q861*
c.2581C>T
1 paper
NM_000535.7
p.I859_S860del2
c.2575_2579del6
1 paper
NM_000535.7
p.M850_S860del11
c.2548_2579del33
1 paper
NM_000535.7
p.S860F
c.2579C>T
1 paper
NM_000535.7
p.S860Y
c.2579C>A
1 paper
NM_000535.7
p.I859delFs
c.2576delA
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