Product Details

SNP ID

rs7840284

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.8:94723750 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TTGATATGTCTTAAAATCAGTGCAC[A/G]CATTCAGTATGACAGTGTGGTTTTT

Phenotype

MIM: 613895

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DPY19L4 PubMed Links

Additional Information

For this assay, SNP(s) [rs76627971] 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

DPY19L4

Gene Name

dpy-19 like 4 (C. elegans)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_181787.2		Intron			NP_861452.2
XM_005250894.4		Intron			XP_005250951.2
XM_005250895.3		Intron			XP_005250952.1
XM_011516983.2		Intron			XP_011515285.1
XM_011516984.2		Intron			XP_011515286.1
XM_017013351.1		Intron			XP_016868840.1
XM_017013352.1		Intron			XP_016868841.1
XM_017013353.1		Intron			XP_016868842.1
XM_017013354.1		Intron			XP_016868843.1
XM_017013355.1		Intron			XP_016868844.1
XM_017013356.1		Intron			XP_016868845.1
XM_017013357.1		Intron			XP_016868846.1

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