Varaico: Literature-Extracted Genetic Variants

Gene:MSH2
Variant:p.M688L

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.M688L
c.2062A>C
Surrounding Variants
5 papers
NM_000251.3
p.M688V
c.2062A>G
1 paper
NM_000251.3
p.M688L
c.2062A>T
6 papers
NM_000251.3
p.L687L
c.2061C>G
1 paper
NM_000251.3
p.M688delFs
c.2062_2063delAT
2 papers
NM_000251.3
p.M688K
c.2063T>A
33 papers
NM_000251.3
p.M688R
c.2063T>G
33 papers
NM_000251.3
p.M688I
c.2064G>A
30 papers
NM_000251.3
p.M688I
c.2064G>C
30 papers
NM_000251.3
p.M688I
c.2064G>T
8 papers
NM_000251.3
p.L687P
c.2060T>C
2 papers
NM_000251.3
p.L687R
c.2060T>G
1 paper
NM_000251.3
p.L687fs
c.2059_2060fs
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."