Product Details

SNP ID

rs17089267

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:68318073 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTAGTCTTTAGTTTGAAAGACAGC[A/G]TACAATTATTTATCATCAAAAATCT

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

YTHDC1 PubMed Links

Additional Information

For this assay, SNP(s) [rs115892907] 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

YTHDC1

Gene Name

YTH domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_005265706.2		Intron			XP_005265763.1
XM_005265707.2		Intron			XP_005265764.1
XM_005265708.2		Intron			XP_005265765.1
XM_017008832.1		Intron			XP_016864321.1
XM_017008833.1		Intron			XP_016864322.1

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