Product Details

SNP ID
rs2553808
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:35142561 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AATTGAGCATTAGAGACTCCGCCCC[C/T]TGCTGGGAGTTAGAACTTTAGCTGT
Phenotype
MIM: 107269
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CD44 PubMed Links
Additional Information
For this assay, SNP(s) [rs75219225] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
CD44
Gene Name
CD44 molecule (Indian blood group)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000610.3 Intron NP_000601.3
NM_001001389.1 Intron NP_001001389.1
NM_001001390.1 Intron NP_001001390.1
NM_001001391.1 Intron NP_001001391.1
NM_001001392.1 Intron NP_001001392.1
NM_001202555.1 Intron NP_001189484.1
NM_001202556.1 Intron NP_001189485.1
NM_001202557.1 Intron NP_001189486.1
XM_005253231.2 Intron XP_005253288.1
XM_005253232.2 Intron XP_005253289.1
XM_005253233.2 Intron XP_005253290.1
XM_005253234.2 Intron XP_005253291.1
XM_005253235.2 Intron XP_005253292.1
XM_005253238.2 Intron XP_005253295.1
XM_005253239.2 Intron XP_005253296.1
XM_005253240.2 Intron XP_005253297.1
XM_006718388.1 Intron XP_006718451.1
XM_006718390.3 Intron XP_006718453.1
XM_011520482.1 Intron XP_011518784.1
XM_011520483.1 Intron XP_011518785.1
XM_011520484.1 Intron XP_011518786.1
XM_011520485.1 Intron XP_011518787.1
XM_011520486.1 Intron XP_011518788.1
XM_011520487.2 Intron XP_011518789.1
XM_011520488.1 Intron XP_011518790.1
XM_011520489.2 Intron XP_011518791.1
XM_017018583.1 Intron XP_016874072.1
XM_017018584.1 Intron XP_016874073.1
XM_017018585.1 Intron XP_016874074.1
Gene
LOC100507144
Gene Name
uncharacterized LOC100507144
There are no transcripts associated with this gene.

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