Product Details

SNP ID
rs112783606
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:45488904 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACTCTGTACCAAATCTCCCAAAGC[A/G]TGTACAAATGCAGCTCTCACTGCCA
Phenotype
MIM: 602095
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC30A4 PubMed Links

Gene Details

Gene
SLC30A4
Gene Name
solute carrier family 30 member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321036.1 949 Intron NP_001307965.1
NM_013309.5 949 Silent Mutation CAC,CAT H277H NP_037441.2
XM_011521997.2 949 Silent Mutation CAC,CAT H277H XP_011520299.1
XM_017022560.1 949 Silent Mutation CAC,CAT H277H XP_016878049.1
XM_017022561.1 949 Intron XP_016878050.1
XM_017022562.1 949 Intron XP_016878051.1

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