Product Details

SNP ID
rs79951667
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:196198074 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAAGAAAAATGTTTTGACCCCAGA[A/G]GTGGTTTGGGCTCAGGGATTGGGAT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HECW2 PubMed Links

Gene Details

Gene
HECW2
Gene Name
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001304840.1 8142 Intron NP_001291769.1
NM_020760.2 8142 Intron NP_065811.1
XM_006712646.3 8142 UTR 3 XP_006712709.1
XM_006712648.3 8142 UTR 3 XP_006712711.1
XM_017004563.1 8142 UTR 3 XP_016860052.1

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