Product Details

SNP ID
rs200519612
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35332822 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGAGACAAGAATAAGAACTGCACA[C/G]TGAGTATCCACCCGGTGCACCTCAA
Phenotype
MIM: 107266
Polymorphism
C/G, Transversion 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_001185099.1 394 Missense Mutation CTG,GTG L104V NP_001172028.1
NM_001185100.1 394 Missense Mutation CTG,GTG L104V NP_001172029.1
NM_001185101.1 394 Missense Mutation CTG,GTG L104V NP_001172030.1
NM_001278417.1 394 UTR 5 NP_001265346.1
NM_001771.3 394 Missense Mutation CTG,GTG L104V NP_001762.2

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