Product Details

SNP ID: rs200056012
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:19145087 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CGTAGGTGATCACCCTTTTCCTCTT[G/T]GGGCGGCCTAATAGGGAGACACCTC
Phenotype
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: FERD3L PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152898.2	335	Silent Mutation	CCA,CCC	P92P	NP_690862.1