Product Details

SNP ID: rs59991531
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:39532705 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCTCACCCTCGGACGCCGCCAGCA[G/T]CTCCAGGCCCCGCCGCAGCAGGGCG
Phenotype: MIM: 610225
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: RPS19BP1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_194326.3	151	Missense Mutation			NP_919307.1