Product Details

SNP ID
rs201597886
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.20:46350488 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGCAGCAGCTCCAGGTCGGGGCTG[A/G]AGCCCAGCCCCTTCAAGGCCTTGGG
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC35C2 PubMed Links

Gene Details

Gene
SLC35C2
Gene Name
solute carrier family 35 member C2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001281457.1 1264 Missense Mutation TCC,TTC S221F NP_001268386.1
NM_001281458.1 1264 Missense Mutation TCC,TTC S364F NP_001268387.1
NM_001281459.1 1264 Missense Mutation TCC,TTC S200F NP_001268388.1
NM_001281460.1 1264 Missense Mutation TCC,TTC S335F NP_001268389.1
NM_015945.11 1264 Missense Mutation TCC,TTC S335F NP_057029.8
NM_173073.3 1264 Missense Mutation TCC,TTC S314F NP_775096.1
NM_173179.3 1264 Missense Mutation TCC,TTC S335F NP_775271.1
XM_011528831.1 1264 Missense Mutation TCC,TTC S335F XP_011527133.1
XM_011528832.1 1264 Missense Mutation TCC,TTC S335F XP_011527134.1
XM_011528833.1 1264 Missense Mutation TCC,TTC S335F XP_011527135.1
XM_011528834.1 1264 Missense Mutation TCC,TTC S334F XP_011527136.1
XM_011528835.1 1264 Missense Mutation TCC,TTC S297F XP_011527137.1
XM_011528836.1 1264 Missense Mutation TCC,TTC S221F XP_011527138.1
XM_011528837.1 1264 Missense Mutation TCC,TTC S221F XP_011527139.1
XM_011528838.1 1264 Missense Mutation TCC,TTC S183F XP_011527140.1
XM_017027856.1 1264 Missense Mutation TCC,TTC S335F XP_016883345.1
XM_017027857.1 1264 Missense Mutation TCC,TTC S335F XP_016883346.1
XM_017027858.1 1264 Missense Mutation TCC,TTC S335F XP_016883347.1
XM_017027859.1 1264 Missense Mutation TCC,TTC S335F XP_016883348.1
XM_017027860.1 1264 Missense Mutation TCC,TTC S335F XP_016883349.1
XM_017027861.1 1264 Missense Mutation TCC,TTC S314F XP_016883350.1
XM_017027862.1 1264 UTR 3 XP_016883351.1

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