Product Details

SNP ID

rs3134296

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:103415313 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAGCGGCGCAGGATCCAGTTGAGC[C/T]AGCAGGCCGCCGCTCCGCGAGTCAC

Phenotype

MIM: 616196 MIM: 610815

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

DCAF13 PubMed Links

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	23	Missense Mutation	CCA,CTA	P108L	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	23	UTR 5			NP_110407.2
XM_017013877.1	23	Intron			XP_016869366.1

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