Product Details

SNP ID
rs201479480
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:100906948 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGTTATTTCAAAATGGAGAGATAA[C/T]GATGCTTTCTCCTATGGGTAAGACT
Phenotype
MIM: 611149
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC30A7 PubMed Links

Gene Details

Gene
SLC30A7
Gene Name
solute carrier family 30 member 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001144884.1 464 Silent Mutation AAC,AAT N93N NP_001138356.1
NM_133496.4 464 Silent Mutation AAC,AAT N93N NP_598003.2
XM_011540779.2 464 Silent Mutation AAC,AAT N23N XP_011539081.1
XM_017000400.1 464 Silent Mutation AAC,AAT N93N XP_016855889.1
XM_017000401.1 464 Silent Mutation AAC,AAT N93N XP_016855890.1

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