Product Details

SNP ID
rs117249984
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:107504696 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAATCACACACCAGTTTCCTTGAT[A/C]GTAGTAGCTTTGCAGAATTCTGACA
Phenotype
MIM: 613306
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
ALKBH8 PubMed Links

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 1872 Missense Mutation NP_001287939.1
NM_138775.2 1872 Missense Mutation NP_620130.2
XM_005271728.2 1872 Missense Mutation XP_005271785.1
XM_005271729.3 1872 Missense Mutation XP_005271786.1
XM_017018553.1 1872 Missense Mutation XP_016874042.1
XM_017018554.1 1872 Missense Mutation XP_016874043.1
XM_017018555.1 1872 Missense Mutation XP_016874044.1
XM_017018556.1 1872 Missense Mutation XP_016874045.1
XM_017018557.1 1872 Intron XP_016874046.1

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