Product Details

SNP ID
rs10056358
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:55630060 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATGTAAACAAGTTTCAGATTCCACG[A/T]TGCAACTCATAAGAAGCTACCACTC
Phenotype
MIM: 616203
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC38A9 PubMed Links

Gene Details

Gene
SLC38A9
Gene Name
solute carrier family 38 member 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001258286.1 Intron NP_001245215.1
NM_001258287.1 Intron NP_001245216.1
NM_001282429.1 Intron NP_001269358.1
NM_173514.3 Intron NP_775785.2
XM_006714537.2 Intron XP_006714600.1
XM_006714538.3 Intron XP_006714601.1
XM_006714539.3 Intron XP_006714602.1
XM_011543173.1 Intron XP_011541475.1
XM_011543174.1 Intron XP_011541476.1
XM_011543176.1 Intron XP_011541478.1
XM_011543177.1 Intron XP_011541479.1
XM_011543178.1 Intron XP_011541480.1
XM_011543180.1 Intron XP_011541482.1
XM_011543182.1 Intron XP_011541484.1
XM_011543183.1 Intron XP_011541485.1
XM_011543184.1 Intron XP_011541486.1
XM_017009077.1 Intron XP_016864566.1
XM_017009078.1 Intron XP_016864567.1
XM_017009079.1 Intron XP_016864568.1
XM_017009080.1 Intron XP_016864569.1
XM_017009081.1 Intron XP_016864570.1
XM_017009082.1 Intron XP_016864571.1

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