Product Details

SNP ID
rs1122524
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:63163285 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTTTTCTCATTCTTCATTACTTAAA[A/C]AATTCCTTTACTTATCACTTCTTTT
Phenotype
MIM: 610792
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SLC22A25 PubMed Links

Gene Details

Gene
SLC22A25
Gene Name
solute carrier family 22 member 25
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_199352.3 2312 Intron NP_955384.3
XM_017017684.1 2312 UTR 3 XP_016873173.1
XM_017017685.1 2312 UTR 3 XP_016873174.1
XM_017017686.1 2312 UTR 3 XP_016873175.1
XM_017017687.1 2312 Intron XP_016873176.1
XM_017017688.1 2312 UTR 3 XP_016873177.1
XM_017017689.1 2312 UTR 3 XP_016873178.1
XM_017017690.1 2312 UTR 3 XP_016873179.1
XM_017017691.1 2312 UTR 3 XP_016873180.1
XM_017017692.1 2312 UTR 3 XP_016873181.1
XM_017017693.1 2312 UTR 3 XP_016873182.1
XM_017017694.1 2312 UTR 3 XP_016873183.1
XM_017017695.1 2312 Intron XP_016873184.1
XM_017017696.1 2312 UTR 3 XP_016873185.1

View Full Product Details