Product Details

SNP ID

rs73551679

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:107503598 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTAACCTAAGTGGTAAGTTAACTGG[G/T]TTACTATTATGCAATATTGTACAGA

Phenotype

MIM: 613306

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

ALKBH8 PubMed Links

Additional Information

For this assay, SNP(s) [rs560973772] 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

ALKBH8

Gene Name

alkB homolog 8, tRNA methyltransferase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001301010.1	2970	UTR 3			NP_001287939.1
NM_138775.2	2970	UTR 3			NP_620130.2
XM_005271728.2	2970	UTR 3			XP_005271785.1
XM_005271729.3	2970	UTR 3			XP_005271786.1
XM_017018553.1	2970	UTR 3			XP_016874042.1
XM_017018554.1	2970	UTR 3			XP_016874043.1
XM_017018555.1	2970	UTR 3			XP_016874044.1
XM_017018556.1	2970	UTR 3			XP_016874045.1
XM_017018557.1	2970	Intron			XP_016874046.1

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