Product Details

SNP ID
rs2274569
Assay Type
Functionally tested
NCBI dbSNP Submissions
28
Location
Chr.1:99969523 on Build GRCh38
Set Membership
HapMap JSNP
Context Sequence [VIC/FAM]
GTCTCAAGATCTCAGTCAGGGTGGG[C/T]GAAGTGGAAGAACAAGCCTTCTTGC
Phenotype
MIM: 605632
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC35A3 PubMed Links

Gene Details

Gene
SLC35A3
Gene Name
solute carrier family 35 member A3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001271684.1 157 Intron NP_001258613.1
NM_001271685.1 157 Intron NP_001258614.1
NM_012243.2 157 Intron NP_036375.1
XM_005270691.4 157 UTR 5 XP_005270748.1
XM_011541135.2 157 Intron XP_011539437.1
XM_011541136.2 157 Intron XP_011539438.1
XM_011541137.2 157 Intron XP_011539439.1
XM_011541138.2 157 Intron XP_011539440.1
XM_017000869.1 157 UTR 5 XP_016856358.1
XM_017000870.1 157 UTR 5 XP_016856359.1
XM_017000871.1 157 UTR 5 XP_016856360.1
XM_017000872.1 157 UTR 5 XP_016856361.1

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