Product Details

SNP ID: rs55969078
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:56113203 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAGTGATGGCAAAGGAATAAATGTC[G/T]GCTTTAGGCGTCACGCCCTCTCCTT
Phenotype: MIM: 190060
Polymorphism: G/T, 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	780	Silent Mutation			NP_005363.1