Product Details

SNP ID

rs897669

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:55263144 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TATTCTCCTCACCCAAAGACTTCAG[A/G]TGCCTCAAAACATAAGAATGTCTAA

Phenotype

MIM: 612720

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DHX29 PubMed Links

Additional Information

For this assay, SNP(s) [rs545988780] 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

DHX29

Gene Name

DEAH-box helicase 29

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019030.2		Intron			NP_061903.2
XM_006714653.2		Intron			XP_006714716.1
XM_017009588.1		Intron			XP_016865077.1

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