Product Details

SNP ID

rs146161228

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:103415111 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGAAGCCGGAGACTCTAGTACTGAG[A/G]GGGCAAGAACGGGGCACAGACACTA

Phenotype

MIM: 616196 MIM: 610815

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DCAF13 PubMed Links

Additional Information

For this assay, SNP(s) [rs3134295] 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

DCAF13

Gene Name

DDB1 and CUL4 associated factor 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015420.6	225	Missense Mutation	AGG,GGG	R41G	NP_056235.4

Gene

SLC25A32

Gene Name

solute carrier family 25 member 32

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030780.4	225	UTR 5			NP_110407.2
XM_017013877.1	225	UTR 5			XP_016869366.1

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