Product Details

SNP ID: rs149352998
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:19145297 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGAGGAGAGGGCGTCTCGGGGAGGC[C/T]AGGGACAGGTCTGCGACGAAGTCCA
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	125	Silent Mutation	CTA,CTG	L22L	NP_690862.1