Product Details

SNP ID
rs1193789
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:63274844 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TATTGCTTTATACCCTGACACATGG[A/G]ATCAATTCCCTTTTACTTGGAATGG
Phenotype
MIM: 607580
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC22A10 PubMed Links

Gene Details

Gene
SLC22A10
Gene Name
solute carrier family 22 member 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039752.3 Intron NP_001034841.3
XM_011545016.2 Intron XP_011543318.1
XM_017017699.1 Intron XP_016873188.1
XM_017017700.1 Intron XP_016873189.1
XM_017017701.1 Intron XP_016873190.1
XM_017017702.1 Intron XP_016873191.1
XM_017017703.1 Intron XP_016873192.1
XM_017017704.1 Intron XP_016873193.1

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