Product Details

SNP ID
rs139372163
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35332740 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCGAAGTTTGATGGGACAAGACT[C/T]TATGAAAGCACAAAGGATGGGAAGG
Phenotype
MIM: 107266
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CD22 PubMed Links

Gene Details

Gene
CD22
Gene Name
CD22 molecule
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001185099.1 312 Silent Mutation CTC,CTT L76L NP_001172028.1
NM_001185100.1 312 Silent Mutation CTC,CTT L76L NP_001172029.1
NM_001185101.1 312 Silent Mutation CTC,CTT L76L NP_001172030.1
NM_001278417.1 312 UTR 5 NP_001265346.1
NM_001771.3 312 Silent Mutation CTC,CTT L76L NP_001762.2

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