Product Details

SNP ID
rs7155084
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:69408478 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGTAAAATAAGACAGCCCCAGTGTC[A/G]TGATATATGGCAGCTGACCTTCAGT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC39A9 PubMed Links

Gene Details

Gene
SLC39A9
Gene Name
solute carrier family 39 member 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001252148.1 Intron NP_001239077.1
NM_001252150.1 Intron NP_001239079.1
NM_001252151.1 Intron NP_001239080.1
NM_001252152.1 Intron NP_001239081.1
NM_018375.4 Intron NP_060845.2
XM_005267834.1 Intron XP_005267891.1
XM_017021426.1 Intron XP_016876915.1

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