Product Details

SNP ID
rs6012753
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:49817712 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTGTCTGTCATAGTTTTAGAAACTT[A/T]TAAACCGATACTGAAAAAGTACACA
Phenotype
MIM: 612730
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC9A8 PubMed Links

Gene Details

Gene
SLC9A8
Gene Name
solute carrier family 9 member A8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001260491.1 Intron NP_001247420.1
NM_015266.2 Intron NP_056081.1
XM_006723756.1 Intron XP_006723819.1
XM_011528736.1 Intron XP_011527038.1
XM_011528737.1 Intron XP_011527039.1
XM_011528738.1 Intron XP_011527040.1
XM_011528739.1 Intron XP_011527041.1
XM_011528740.1 Intron XP_011527042.1
XM_011528741.1 Intron XP_011527043.1
XM_011528742.1 Intron XP_011527044.1
XM_011528743.2 Intron XP_011527045.1
XM_011528744.2 Intron XP_011527046.1
XM_011528745.1 Intron XP_011527047.1
XM_017027754.1 Intron XP_016883243.1
XM_017027755.1 Intron XP_016883244.1
XM_017027756.1 Intron XP_016883245.1

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