Product Details

SNP ID
rs12559112
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:135989232 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGTTTCTAGATTGTAATATAGATCA[A/G]TTGCTCCAGTTACAAACACACAATT
Phenotype
MIM: 300231
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC9A6 PubMed Links

Gene Details

Gene
SLC9A6
Gene Name
solute carrier family 9 member A6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001042537.1 Intron NP_001036002.1
NM_001177651.1 Intron NP_001171122.1
NM_006359.2 Intron NP_006350.1
XM_006724726.3 Intron XP_006724789.1
XM_011531243.2 Intron XP_011529545.1
XM_017029223.1 Intron XP_016884712.1
XM_017029224.1 Intron XP_016884713.1
XM_017029225.1 Intron XP_016884714.1

View Full Product Details