Product Details

SNP ID
rs74048377
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:2903797 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGCTGTTCCTCCTGCCTCTCACCC[A/G]GCAGCCTTTGCCCTCTGGAGTCCCT
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 1708 Intron NP_001302430.1
NM_001315502.1 1708 Intron NP_001302431.1
NM_002555.5 1708 Intron NP_002546.3
NM_183233.2 1708 Intron NP_899056.2
XM_011520141.2 1708 Intron XP_011518443.2
XM_011520142.2 1708 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 1708 UTR 5 NP_001289791.1
NM_007105.3 1708 UTR 5 NP_009036.2
XM_017017832.1 1708 UTR 5 XP_016873321.1
XM_017017833.1 1708 UTR 5 XP_016873322.1
XM_017017834.1 1708 UTR 5 XP_016873323.1
XM_017017835.1 1708 Intron XP_016873324.1
XM_017017836.1 1708 Intron XP_016873325.1

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