Product Details

SNP ID
rs112153242
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:2726360 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGCTTACCAGAAAAAGAAGCTATG[C/G]TTCAAAGAAAATGGTAAGTCTCAGT
Phenotype
MIM: 313470 MIM: 450000
Polymorphism
C/G, 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_001122898.2 639 Missense Mutation TGC,TGG C138W NP_001116370.1
NM_001321367.1 639 Missense Mutation TGC,TGG C154W NP_001308296.1
NM_001321368.1 639 Missense Mutation TGC,TGG C154W NP_001308297.1
NM_001321369.1 639 Missense Mutation TGC,TGG C138W NP_001308298.1
NM_001321370.1 639 Missense Mutation TGC,TGG C137W NP_001308299.1
NM_002414.4 639 Missense Mutation TGC,TGG C154W NP_002405.1

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