Product Details

SNP ID
rs199988288
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:17953342 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTTTCTTCTACTCAGCCGTGTTTT[A/T]TCTACTGAGACAGACAAACCCTCAG
Phenotype
MIM: 608734
Polymorphism
A/T, Transversion 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_001145195.1 339 Missense Mutation TTA,TTT L22F NP_001138667.1
NM_001282733.1 339 Missense Mutation TTA,TTT L22F NP_001269662.1
NM_001282734.1 339 Intron NP_001269663.1
NM_152725.3 339 Missense Mutation TTA,TTT L22F NP_689938.2

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