Product Details

SNP ID
rs140688356
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:2723358 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGAGGCAGCCACAGGAAAGAAGGG[A/G]AAGAGGGTAGGTGCACCTGGCTTCT
Phenotype
MIM: 313470 MIM: 450000
Polymorphism
A/G, Transition 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_001122898.2 535 Missense Mutation AAA,GAA K103E NP_001116370.1
NM_001321367.1 535 Missense Mutation AAA,GAA K119E NP_001308296.1
NM_001321368.1 535 Missense Mutation AAA,GAA K119E NP_001308297.1
NM_001321369.1 535 Missense Mutation AAA,GAA K103E NP_001308298.1
NM_001321370.1 535 Intron NP_001308299.1
NM_002414.4 535 Missense Mutation AAA,GAA K119E NP_002405.1

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