Product Details

SNP ID
rs184274661
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:2726344 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCATCTCTAGCTTCATTGCTTACC[A/C]GAAAAAGAAGCTATGCTTCAAAGAA
Phenotype
MIM: 313470 MIM: 450000
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CD99 PubMed Links

Gene Details

Gene
CD99
Gene Name
CD99 molecule
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001122898.2 623 Missense Mutation CAG,CCG Q133P NP_001116370.1
NM_001321367.1 623 Missense Mutation CAG,CCG Q149P NP_001308296.1
NM_001321368.1 623 Missense Mutation CAG,CCG Q149P NP_001308297.1
NM_001321369.1 623 Missense Mutation CAG,CCG Q133P NP_001308298.1
NM_001321370.1 623 Missense Mutation CAG,CCG Q132P NP_001308299.1
NM_002414.4 623 Missense Mutation CAG,CCG Q149P NP_002405.1

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