Product Details

SNP ID: rs35074823
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:56113212 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAAAGGAATAAATGTCGGCTTTAGG[C/G]GTCACGCCCTCTCCTTTCAGGAGCT
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	771	Silent Mutation	ACC,ACG	T257T	NP_005363.1