Product Details

SNP ID
rs150575910
Assay Type
Functionally Tested
NCBI dbSNP Submissions
9
Location
Chr.1:171783869 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATGAAGGAATGTAATGCCACCCGA[C/T]GGCCCCAGATGAGCTTCTTGAAGAT
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
METTL13 PubMed Links
Additional Information
For this assay, SNP(s) [rs2232816] 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
METTL13
Gene Name
methyltransferase like 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001007239.1 297 Missense Mutation CGG,TGG R95W NP_001007240.1
NM_014955.2 297 Missense Mutation CGG,TGG R9W NP_055770.1
NM_015935.4 297 Missense Mutation CGG,TGG R95W NP_057019.3
XM_017001455.1 297 Missense Mutation CGG,TGG R9W XP_016856944.1
XM_017001456.1 297 Missense Mutation CGG,TGG R9W XP_016856945.1
XM_017001457.1 297 Missense Mutation CGG,TGG R9W XP_016856946.1
XM_017001458.1 297 Missense Mutation CGG,TGG R95W XP_016856947.1
XM_017001459.1 297 Missense Mutation CGG,TGG R9W XP_016856948.1

View Full Product Details