Product Details

SNP ID
rs389646
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:2904531 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGTAATAACAGTCCCTCCCTGTAGG[A/G]TTGGTGCGGGGAAGAGTGAATGAGA
Phenotype
MIM: 602631 MIM: 603240
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC22A18 PubMed Links

Gene Details

Gene
SLC22A18
Gene Name
solute carrier family 22 member 18
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001315501.1 974 Intron NP_001302430.1
NM_001315502.1 974 Intron NP_001302431.1
NM_002555.5 974 Intron NP_002546.3
NM_183233.2 974 Intron NP_899056.2
XM_011520141.2 974 Intron XP_011518443.2
XM_011520142.2 974 Intron XP_011518444.2
Gene
SLC22A18AS
Gene Name
solute carrier family 22 member 18 antisense
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001302862.1 974 Intron NP_001289791.1
NM_007105.3 974 Intron NP_009036.2
XM_017017832.1 974 UTR 5 XP_016873321.1
XM_017017833.1 974 UTR 5 XP_016873322.1
XM_017017834.1 974 UTR 5 XP_016873323.1
XM_017017835.1 974 Intron XP_016873324.1
XM_017017836.1 974 Intron XP_016873325.1

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