Product Details

SNP ID: rs146964611
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:56113077 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCCCGGGGAGCGAGTCCTCGAAGAC[C/G]GCAGCGGAGAGGGACGGGCGCAGGT
Phenotype: MIM: 190060
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: MOS PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005372.1	906	Silent Mutation	GCC,GCG	A302A	NP_005363.1