Product Details

SNP ID
rs9819572
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:136831706 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATAATCTCAAGTTGTAAACAAATGG[C/T]TTGGAATGTGACAGCCTGGGTTTGA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC35G2 PubMed Links

Gene Details

Gene
SLC35G2
Gene Name
solute carrier family 35 member G2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001097599.1 897 Intron NP_001091068.1
NM_001097600.1 897 Intron NP_001091069.1
NM_025246.2 897 Intron NP_079522.2
XM_006713773.3 897 Intron XP_006713836.1
XM_011513214.2 897 UTR 5 XP_011511516.1
XM_017007289.1 897 Intron XP_016862778.1
XM_017007290.1 897 Intron XP_016862779.1
XM_017007291.1 897 Intron XP_016862780.1

View Full Product Details