Product Details

SNP ID: rs112344790
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:23439494 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAGCAGCGTCTGCACCCACTACCCC[A/G]CCGGGGCCCCGGGTCCCACGGCCGC
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	226	Missense Mutation	ACC,GCC	T13A	NP_001138845.1