Varaico: Literature-Extracted Genetic Variants

Gene:MSH2
Variant:p.L387fs

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.L387fs
c.1159_1160fs
Surrounding Variants
5 papers
NM_000251.3
p.L387V
c.1159C>G
2 papers
NM_000251.3
p.L387F
c.1159C>T
1 paper
NM_000251.3
p.L387H
c.1160T>A
1 paper
NM_000251.3
p.D386D
c.1158T>C
1 paper
NM_000251.3
p.L387P
c.1160T>C
1 paper
NM_000251.3
p.L387R
c.1160T>G
1 paper
NM_000251.3
p.L387delFs
c.1159delC
11 papers
NM_000251.3
p.L387_N388del2
c.1159_1163del6
1 paper
NM_000251.3
p.L387_R389Fs
c.1160_1166delinsCATAAFs
2 papers
NM_000251.3
p.D386G
c.1157A>G
3 papers
NM_000251.3
p.N388insFs
c.1163_1164insA
17 papers
NM_000251.3
p.N388_R389del2
c.1162_1166del6
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