Product Details

SNP ID
rs12291397
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:45805904 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAGGCCAACGGGGAGAAGCCCTTT[C/T]TGCTGCGGGCATTGCAGATCGCGCT
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_001145265.1 815 Silent Mutation CTG,TTG L22L NP_001138737.1
NM_001145266.1 815 Silent Mutation CTG,TTG L22L NP_001138738.1
NM_018389.4 815 Silent Mutation CTG,TTG L35L NP_060859.4
XM_011520202.2 815 Intron XP_011518504.1
XM_011520203.2 815 Silent Mutation CTG,TTG L35L XP_011518505.1

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