Product Details

SNP ID
rs200858797
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:8605226 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCCCTTTCGCACCTTTGAAGGTC[A/G]TGATGGCTATTTGCACCCCGGCGCG
Phenotype
MIM: 605257
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
AICDA PubMed Links

Gene Details

Gene
AICDA
Gene Name
activation-induced cytidine deaminase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020661.2 614 Missense Mutation NP_065712.1
XM_011520772.2 614 Missense Mutation ACG,ATG T139M XP_011519074.1
XM_011520773.2 614 Missense Mutation ACG,ATG T139M XP_011519075.1

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