Product Details

SNP ID: rs1108975
Assay Type: Functionally tested
NCBI dbSNP Submissions: 36
Location: Chr.1:19921868 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AAATGGGTCCAGCCTGACAGTCCCA[G/T]TGAGGAGTCAGCCTTTGGAAACAGC
Phenotype: MIM: 611758
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: OTUD3 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014589.2		Intron			NP_055404.1