Product Details

SNP ID
rs6598903
Assay Type
Functionally tested
NCBI dbSNP Submissions
25
Location
Chr.1:27782169 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CAGGATGTGCCAGTAGTACAGTGGT[A/G]CCGTCATAGGTCACTGCAACCTTGA
Phenotype
MIM: 606892
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
STX12 PubMed Links

Gene Details

Gene
STX12
Gene Name
syntaxin 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_177424.2 Intron NP_803173.1

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