Varaico: Literature-Extracted Genetic Variants

Gene:MSH2
Variant:p.S168insFs

MSH2

3,750 papers

RefSeq Summary

This locus is frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). When cloned, it was discovered to be a human homolog of the E. coli mismatch repair gene mutS, consistent with the cha...

Pfam Domains

MutS_Iaa 17–132UCSCMutS domain I
MutS_IIaa 145–290UCSCMutS domain II
MutS_IIIaa 305–609UCSCMutS domain III
MutS_IVaa 473–569UCSCMutS family domain IV
MutS_Vaa 665–852UCSCMutS domain V

Gene Aliases

HGNC Name

mutS homolog 2

HGNC Previous Symbol

COCA1

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
1 paper
NM_000251.3
p.S168insFs
c.503dupC
Surrounding Variants
1 paper
NM_000251.3
p.S168P
c.502T>C
1 paper
NM_000251.3
p.S168delFs
c.503delC
1 paper
NM_000251.3
p.S168Y
c.503C>A
2 papers
NM_000251.3
p.S168F
c.503C>T
3 papers
NM_000251.3
p.I169_Q170delFs
c.506_509del4
1 paper
NM_000251.3
p.D167D
c.501T>C
1 paper
NM_000251.3
p.D167_S168insFs
c.501_502insA
1 paper
NM_000251.3
p.S168delFs
c.502_503delTC
1 paper
NM_000251.3
p.D167V
c.500A>T
1 paper
NM_000251.3
p.S168_I169insFs
c.504_505insA
1 paper
NM_000251.3
p.S168S
c.504C>T
1 paper
NM_000251.3
p.I169delFs
c.505delA
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."