Product Details

SNP ID
rs3796228
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:143265869 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAGAGCAACACAGGCTGCAGAATCC[C/T]ACCCTCCAGCATATCGCGGGGAGGG
Phenotype
MIM: 608396
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC9A9 PubMed Links

Gene Details

Gene
SLC9A9
Gene Name
solute carrier family 9 member A9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_173653.3 2980 UTR 3 NP_775924.1
XM_011512703.2 2980 Intron XP_011511005.1
XM_011512704.2 2980 Intron XP_011511006.1
XM_017006202.1 2980 Intron XP_016861691.1
XM_017006203.1 2980 Intron XP_016861692.1

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