Product Details

SNP ID
rs139905034
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:52768158 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTTCAGATAGGGAACTCACAGAC[G/T]GCCAGATGGGAGGTGGAGCAGGGGA
Phenotype
MIM: 154545
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
MBL2 PubMed Links

Gene Details

Gene
MBL2
Gene Name
mannose binding lectin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000242.2 859 Silent Mutation GCA,GCC A242A NP_000233.1
XM_006717861.3 859 Silent Mutation GCA,GCC A242A XP_006717924.1
XM_011539816.2 859 Silent Mutation GCA,GCC A242A XP_011538118.1

View Full Product Details