Product Details

SNP ID: rs145174585
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:19145349 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CACCGTAGTGTCCACGCAGCTCTCC[C/G]GATAGGCCGCCATCGCTTCGGCTTG
Phenotype
Polymorphism: C/G, 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	73	Missense Mutation	CCG,CGG	P5R	NP_690862.1