Product Details

SNP ID
rs17157906
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:63164352 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TACTGCATTAAAAGACTTAATGCAG[C/T]GTCTGGAACAAAGTCAGCTTGATAT
Phenotype
MIM: 610792
Polymorphism
C/T, Transition 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 Intron NP_955384.3
XM_017017684.1 Intron XP_016873173.1
XM_017017685.1 Intron XP_016873174.1
XM_017017686.1 Intron XP_016873175.1
XM_017017687.1 Intron XP_016873176.1
XM_017017688.1 Intron XP_016873177.1
XM_017017689.1 Intron XP_016873178.1
XM_017017690.1 Intron XP_016873179.1
XM_017017691.1 Intron XP_016873180.1
XM_017017692.1 Intron XP_016873181.1
XM_017017693.1 Intron XP_016873182.1
XM_017017694.1 Intron XP_016873183.1
XM_017017695.1 Intron XP_016873184.1
XM_017017696.1 Intron XP_016873185.1

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