Product Details

SNP ID
rs1064457
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:1050557 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCCCAGGGCGGGGGCAGAGCTGA[C/G]CCCTCAGGAGGTGGTTTCGTGTGCA
Phenotype
MIM: 604879
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SLC12A7 PubMed Links

Gene Details

Gene
SLC12A7
Gene Name
solute carrier family 12 member 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006598.2 5121 UTR 3 NP_006589.2
XM_005248231.3 5121 UTR 3 XP_005248288.1
XM_011513939.2 5121 UTR 3 XP_011512241.1
XM_011513940.2 5121 UTR 3 XP_011512242.1
XM_011513941.2 5121 UTR 3 XP_011512243.2
XM_017008958.1 5121 UTR 3 XP_016864447.1
XM_017008959.1 5121 UTR 3 XP_016864448.1

View Full Product Details