Product Details

SNP ID
rs137980785
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:38266074 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCTGCTGAACAGCTGGTACTGAGC[A/G]TGCCCCTGGACACTGCAGGTCACCC
Phenotype
MIM: 604047
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC22A13 PubMed Links

Gene Details

Gene
SLC22A13
Gene Name
solute carrier family 22 member 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004256.3 169 Missense Mutation ATG,GTG M72V NP_004247.2
XM_017007519.1 169 UTR 5 XP_016863008.1

View Full Product Details