Product Details

SNP ID
rs74587373
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:65624338 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCCTTCAAAACCTAGCTCCGAAAT[G/T]GGGGGTAAGATGCTGGTACCCCAAG
Phenotype
MIM: 603617
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC24A1 PubMed Links

Gene Details

Gene
SLC24A1
Gene Name
solute carrier family 24 member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001254740.1 519 Intron NP_001241669.1
NM_001301031.1 519 Missense Mutation ATG,ATT M86I NP_001287960.1
NM_001301032.1 519 Missense Mutation ATG,ATT M86I NP_001287961.1
NM_001301033.1 519 Missense Mutation ATG,ATT M86I NP_001287962.1
NM_004727.2 519 Missense Mutation ATG,ATT M86I NP_004718.1
XM_005254778.3 519 Missense Mutation ATG,ATT M86I XP_005254835.1
XM_005254781.3 519 Missense Mutation ATG,ATT M86I XP_005254838.1
XM_006720768.3 519 Missense Mutation ATG,ATT M86I XP_006720831.1
XM_011522219.1 519 Missense Mutation ATG,ATT M86I XP_011520521.1
XM_011522220.2 519 Missense Mutation ATG,ATT M86I XP_011520522.1
XM_011522221.2 519 Missense Mutation ATG,ATT M86I XP_011520523.1
XM_011522222.2 519 Missense Mutation ATG,ATT M86I XP_011520524.1
XM_011522226.2 519 Missense Mutation ATG,ATT M86I XP_011520528.1
XM_017022724.1 519 Missense Mutation ATG,ATT M86I XP_016878213.1
XM_017022725.1 519 Missense Mutation ATG,ATT M86I XP_016878214.1

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