Product Details

SNP ID
rs143461929
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:63370321 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCAAACATGAGGCCAGAGAAGTGT[C/T]GTCGCTTTGTTCATCCTCAGTGGCA
Phenotype
MIM: 607579
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC22A9 PubMed Links

Gene Details

Gene
SLC22A9
Gene Name
solute carrier family 22 member 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_080866.2 533 Missense Mutation CGT,TGT R89C NP_543142.2
XM_017017159.1 533 Missense Mutation CGT,TGT R89C XP_016872648.1
XM_017017160.1 533 UTR 5 XP_016872649.1

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