Product Details

SNP ID

rs10140164

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:54939405 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCAGTGCCTATTCACTTGTTCTCC[A/G]AAATAAATCTGTAAAGTAACCTCCT

Phenotype

MIM: 608126

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

WDHD1 PubMed Links

Additional Information

For this assay, SNP(s) [rs79245615] 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

WDHD1

Gene Name

WD repeat and HMG-box DNA binding protein 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001008396.2	5472	UTR 3			NP_001008397.1
NM_007086.3	5472	UTR 3			NP_009017.1
XM_006720012.2	5472	UTR 3			XP_006720075.1
XM_011536373.2	5472	Intron			XP_011534675.1
XM_017020940.1	5472	Intron			XP_016876429.1
XM_017020941.1	5472	UTR 3			XP_016876430.1

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