Product Details

SNP ID
rs142477308
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35332594 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGACTCAAGTAAATGGGTTTTTGAG[C/T]ACCCTGAAACCCTCTACGCCTGGGA
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_001185099.1 166 Missense Mutation CAC,TAC H28Y NP_001172028.1
NM_001185100.1 166 Missense Mutation CAC,TAC H28Y NP_001172029.1
NM_001185101.1 166 Missense Mutation CAC,TAC H28Y NP_001172030.1
NM_001278417.1 166 UTR 5 NP_001265346.1
NM_001771.3 166 Missense Mutation CAC,TAC H28Y NP_001762.2

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