Product Details

SNP ID

rs17144719

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:118840712 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGCACATTTTTAAAAACAAGTACAG[C/T]AGGAAATCCTGCTTTTCAGTGAGCC

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

DTWD2 PubMed Links

Additional Information

For this assay, SNP(s) [rs77054799] 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

DTWD2

Gene Name

DTW domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308081.1	2589	UTR 3			NP_001295010.1
NM_173666.3	2589	UTR 3			NP_775937.1
XM_011543338.2	2589	UTR 3			XP_011541640.2
XM_011543340.2	2589	UTR 3			XP_011541642.1

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