Product Details

SNP ID
rs140329485
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:38266177 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCCTCAGCCACCGCTTCAATGAGA[C/T]GCAGCCTTGTGATATGGGCTGGGAA
Phenotype
MIM: 604047
Polymorphism
C/T, 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_004256.3 272 Missense Mutation ACG,ATG T106M NP_004247.2
XM_017007519.1 272 UTR 5 XP_016863008.1

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