Product Details

SNP ID
rs118083022
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:46349622 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATAGACATTATCCCCATTTCACAGA[C/T]TAAAAAACTACGGCACAGACAGGTT
Phenotype
Polymorphism
C/T, 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 2215 UTR 3 NP_001268386.1
NM_001281458.1 2215 UTR 3 NP_001268387.1
NM_001281459.1 2215 UTR 3 NP_001268388.1
NM_001281460.1 2215 UTR 3 NP_001268389.1
NM_015945.11 2215 UTR 3 NP_057029.8
NM_173073.3 2215 UTR 3 NP_775096.1
NM_173179.3 2215 UTR 3 NP_775271.1
XM_011528831.1 2215 Intron XP_011527133.1
XM_011528832.1 2215 Intron XP_011527134.1
XM_011528833.1 2215 Intron XP_011527135.1
XM_011528834.1 2215 Intron XP_011527136.1
XM_011528835.1 2215 Intron XP_011527137.1
XM_011528836.1 2215 Intron XP_011527138.1
XM_011528837.1 2215 Intron XP_011527139.1
XM_011528838.1 2215 Intron XP_011527140.1
XM_017027856.1 2215 Intron XP_016883345.1
XM_017027857.1 2215 Intron XP_016883346.1
XM_017027858.1 2215 Intron XP_016883347.1
XM_017027859.1 2215 Intron XP_016883348.1
XM_017027860.1 2215 Intron XP_016883349.1
XM_017027861.1 2215 Intron XP_016883350.1
XM_017027862.1 2215 Intron XP_016883351.1

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