Product Details

SNP ID: rs139603599
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:19145150 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTTCCTCCTCCTCTTCTCCGTCCCC[C/T]TGGTCCACTTCGCACTCCTCTTCTT
Phenotype
Polymorphism: C/T, Transition 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	272	Silent Mutation	CAA,CAG	Q71Q	NP_690862.1