Product Details

SNP ID

rs181808385

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:159248378 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTATAGCATCACACATACCTGATG[C/T]GATGACCGGATCTTTCATAAGTTCT

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

WDSUB1 PubMed Links

Additional Information

For this assay, SNP(s) [rs73004952] are located under a probe 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

WDSUB1

Gene Name

WD repeat, sterile alpha motif and U-box domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128212.2	1232	Missense Mutation	ACA,GCA	T423A	NP_001121684.1
NM_001128213.1	1232	Missense Mutation	ACA,GCA	T423A	NP_001121685.1
NM_001307994.1	1232	Missense Mutation	ACA,GCA	T331A	NP_001294923.1
NM_152528.2	1232	Missense Mutation	ACA,GCA	T423A	NP_689741.2
XM_005246355.2	1232	Intron			XP_005246412.2
XM_006712341.3	1232	Missense Mutation	ACA,GCA	T254A	XP_006712404.1
XM_011510753.2	1232	Missense Mutation	ACA,GCA	T423A	XP_011509055.1
XM_011510754.2	1232	Missense Mutation	ACA,GCA	T336A	XP_011509056.1
XM_017003481.1	1232	Missense Mutation	ACA,GCA	T423A	XP_016858970.1
XM_017003482.1	1232	Missense Mutation	ACA,GCA	T300A	XP_016858971.1
XM_017003483.1	1232	Missense Mutation	ACA,GCA	T185A	XP_016858972.1

View Full Product Details