Product Details

SNP ID

rs12099195

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:122844938 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTGTTGGTGAAATCTAAAATAAC[A/G]CATTTGGGGGAAGAGAATCAAGAGT

Phenotype

MIM: 612597

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CRTAM PubMed Links

Additional Information

For this assay, SNP(s) [rs116040023] 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

CRTAM

Gene Name

cytotoxic and regulatory T-cell molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001304782.1		Intron			NP_001291711.1
NM_019604.3		Intron			NP_062550.2
XM_011542900.2		Intron			XP_011541202.1

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