Product Details

SNP ID: rs201551577
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:19144992 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGCAAACGTGGGCACCTTCCTCCGC[A/G]GCTGGTCAAAGGCCTCGTTGAGGTT
Phenotype
Polymorphism: A/G, 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	430	Missense Mutation	CCG,CTG	P124L	NP_690862.1