Product Details

SNP ID
rs189405956
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:45806110 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCGCCTGCTGCCCTGGTGCCGTGGA[C/T]TTCCCCAGCTTGCGCCTGGACCTCA
Phenotype
MIM: 605881
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC35C1 PubMed Links

Gene Details

Gene
SLC35C1
Gene Name
solute carrier family 35 member C1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145265.1 1021 Silent Mutation GAC,GAT D90D NP_001138737.1
NM_001145266.1 1021 Silent Mutation GAC,GAT D90D NP_001138738.1
NM_018389.4 1021 Silent Mutation GAC,GAT D103D NP_060859.4
XM_011520202.2 1021 Intron XP_011518504.1
XM_011520203.2 1021 Silent Mutation GAC,GAT D103D XP_011518505.1

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