Product Details

SNP ID
rs141189708
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:223597859 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGGCAGCTTTGGGAAGCTGGTTC[A/G]ATCTAGATCTTCCAGCACCATAAGG
Phenotype
MIM: 118930
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SCG2 PubMed Links

Gene Details

Gene
SCG2
Gene Name
secretogranin II
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003469.4 1653 Missense Mutation TCG,TTG S475L NP_003460.2

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