Product Details

SNP ID: rs1511822
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:23440594 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAGACGGGGCATGGGCCGGGTACCC[A/G]GAGTTGCTGGCCATGGGGCAGATGC
Phenotype: MIM: 612022
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: OTUD1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145373.2	1326	Silent Mutation	CCA,CCG	P379P	NP_001138845.1