Product Details

SNP ID
rs3134295
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:103415131 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTGAGGGGGCAAGAACGGGGCACAG[A/C]CACTACGTCACGCCGGCGGAAAGCG
Phenotype
MIM: 616196 MIM: 610815
Polymorphism
A/C, Transversion 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_015420.6 205 Missense Mutation AGA,AGC R47S 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_030780.4 205 UTR 5 NP_110407.2
XM_017013877.1 205 UTR 5 XP_016869366.1

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