Product Details

SNP ID

rs1385615

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:176072032 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAAGTAGAACTGCCATAATGACCT[C/T]ATTCTTCTCTACTTGCTACCTAATC

Phenotype

MIM: 609005

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

WDR17 PubMed Links

Additional Information

For this assay, SNP(s) [rs79466523] 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

WDR17

Gene Name

WD repeat domain 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_170710.4		Intron			NP_733828.2
NM_181265.3		Intron			NP_851782.3
XM_005262725.3		Intron			XP_005262782.1
XM_011531582.2		Intron			XP_011529884.1
XM_017007686.1		Intron			XP_016863175.1
XM_017007687.1		Intron			XP_016863176.1
XM_017007688.1		Intron			XP_016863177.1
XM_017007689.1		Intron			XP_016863178.1
XM_017007690.1		Intron			XP_016863179.1
XM_017007691.1		Intron			XP_016863180.1
XM_017007692.1		Intron			XP_016863181.1
XM_017007693.1		Intron			XP_016863182.1
XM_017007694.1		Intron			XP_016863183.1
XM_017007695.1		Intron			XP_016863184.1
XM_017007696.1		Intron			XP_016863185.1
XM_017007697.1		Intron			XP_016863186.1

View Full Product Details