Product Details

SNP ID: rs2267433
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:41481768 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GTTTGAAAGCACAATCCAGAAGGCC[A/G]GTGGTCGTGTCACGGCTCTGCCTTC
Phenotype: MIM: 100850
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: ACO2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001098.2		Intron			NP_001089.1
XM_017028812.1		Intron			XP_016884301.1