Product Details

SNP ID
rs904869
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:195581802 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAGTAACCCATGATTGTGCCATTGC[A/G]CTCTAGCATGGGCAGCAGAACAAGA
Phenotype
MIM: 608733
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC39A10 PubMed Links

Gene Details

Gene
SLC39A10
Gene Name
solute carrier family 39 member 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127257.1 Intron NP_001120729.1
NM_020342.2 Intron NP_065075.1
XM_005246689.4 Intron XP_005246746.2
XM_011511504.2 Intron XP_011509806.1
XM_011511505.2 Intron XP_011509807.1
XM_011511506.2 Intron XP_011509808.1
XM_011511507.2 Intron XP_011509809.1
XM_017004522.1 Intron XP_016860011.1
XM_017004523.1 Intron XP_016860012.1

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