Product Details

SNP ID

rs1833679

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:113517415 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTGCATTCTAAACAGCTAACTTA[G/T]AAAAGCAGTCCATTAGAGTAGACTT

Phenotype

MIM: 616530

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

YTHDC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs115501702] 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

YTHDC2

Gene Name

YTH domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022828.3		Intron			NP_073739.3
XM_011543581.1		Intron			XP_011541883.1
XM_011543582.2		Intron			XP_011541884.1
XM_011543586.2		Intron			XP_011541888.1
XM_017009730.1		Intron			XP_016865219.1
XM_017009731.1		Intron			XP_016865220.1
XM_017009732.1		Intron			XP_016865221.1
XM_017009733.1		Intron			XP_016865222.1
XM_017009734.1		Intron			XP_016865223.1
XM_017009735.1		Intron			XP_016865224.1

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