Product Details

SNP ID

rs2077947

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.7:135238353 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CAGCCCTGGCGGCTCCTAGAGGCGA[C/G]TGGTGGGAAGTCTGCCCCCTATGGG

Phenotype

MIM: 609987

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

STRA8 PubMed Links

Additional Information

For this assay, SNP(s) [rs117917236] are located under a probe 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

STRA8

Gene Name

stimulated by retinoic acid 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182489.1		Intron			NP_872295.1
XM_011516137.2		Intron			XP_011514439.1
XM_011516138.2		Intron			XP_011514440.1
XM_011516139.2		Intron			XP_011514441.1
XM_017012150.1		Intron			XP_016867639.1

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