Product Details

SNP ID
rs10764176
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:17953382 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CAAACCCTCAGCCCAGGATAGCAGA[A/G]GCCGTGGGAGTTCAGGCCAACCGGC
Phenotype
MIM: 608734
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC39A12 PubMed Links

Gene Details

Gene
SLC39A12
Gene Name
solute carrier family 39 member 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145195.1 379 Missense Mutation AGC,GGC S36G NP_001138667.1
NM_001282733.1 379 Missense Mutation AGC,GGC S36G NP_001269662.1
NM_001282734.1 379 Intron NP_001269663.1
NM_152725.3 379 Missense Mutation AGC,GGC S36G NP_689938.2

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