Product Details

SNP ID: rs1108974
Assay Type: Functionally tested
NCBI dbSNP Submissions: 55
Location: Chr.1:19922216 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGCTCTGATAAGGCCCAAGGTCACC[A/G]TCAGGAGGGGCTTCCTGTCTTAAGC
Phenotype: MIM: 611758
Polymorphism: A/G, Transition 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