Product Details

SNP ID
rs12269546
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:99614394 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGAGGGGCGGCTAATTTTTTTATA[C/G]TTTTTCAGACTATCTGGCAATGGTG
Phenotype
MIM: 609767
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SLC25A28 PubMed Links

Gene Details

Gene
SLC25A28
Gene Name
solute carrier family 25 member 28
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_031212.3 Intron NP_112489.3
XM_005270208.1 Intron XP_005270265.1
XM_005270211.4 Intron XP_005270268.1
XM_006718005.3 Intron XP_006718068.1
XM_006718006.3 Intron XP_006718069.1
XM_011540239.2 Intron XP_011538541.1
XM_011540240.1 Intron XP_011538542.1
XM_011540244.2 Intron XP_011538546.1
XM_017016741.1 Intron XP_016872230.1
XM_017016742.1 Intron XP_016872231.1

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