AIFM3

AIF family member 3

Summary

Predicted to enable oxidoreductase activity, acting on NAD(P)H. Involved in execution phase of apoptosis. Located in cytosol; endoplasmic reticulum; and mitochondrial inner membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants43 total

rsidPosition (GRCh37)AllelesClassClinVar
rs77120330322:21,327,635G/A—uncertain significance
rs251858598322:21,327,647A/C—uncertain significance
rs37308820722:21,327,653C/T—uncertain significance
rs75134586622:21,327,658A/T—uncertain significance
rs75575671222:21,327,703C/T—uncertain significance
rs77125640022:21,327,725G/T—uncertain significance
rs36760063822:21,328,111G/T—uncertain significance
rs37592889022:21,328,114C/G—uncertain significance
rs251858745922:21,328,123A/G—uncertain significance
rs251858758022:21,328,144C/T—uncertain significance
rs37036225222:21,328,363C/T—uncertain significance
rs75399047822:21,328,369C/T—uncertain significance
rs192350727122:21,328,887C/T—uncertain significance
rs148897148922:21,328,896T/A—uncertain significance
rs14006274922:21,329,013G/A—uncertain significance
rs76899628522:21,329,026G/A—uncertain significance
rs75558947622:21,329,071G/A—uncertain significance
rs251859022722:21,329,100A/T—uncertain significance
rs93047565322:21,330,708T/A—uncertain significance
rs77665099422:21,330,737G/A—uncertain significance
rs76450517922:21,330,748C/T—likely benign
rs75190338322:21,330,749C/T—uncertain significance
rs15080108922:21,330,750G/A—uncertain significance
rs77259248422:21,330,773G/A—uncertain significance
rs18533833222:21,330,800G/A—uncertain significance
rs53358071522:21,330,809G/A—uncertain significance
rs77523412022:21,330,973C/T—uncertain significance
rs75671749022:21,331,003A/T—uncertain significance
rs37347326922:21,331,006C/T—uncertain significance
rs37109862922:21,331,012T/G—uncertain significance
rs77226342422:21,331,033G/A—uncertain significance
rs76267661722:21,331,042G/A—uncertain significance
rs75166241022:21,331,186A/G—uncertain significance
rs14588364022:21,331,187T/G—uncertain significance
rs14661140022:21,331,324A/G—uncertain significance
rs37482361022:21,331,354G/A—uncertain significance
rs73952522:21,332,441T/Cupstream gene variant—
rs36793754722:21,333,628G/A—uncertain significance
rs75600466422:21,333,640A/G—uncertain significance
rs74779841422:21,333,919A/G—uncertain significance
rs37749497222:21,333,921G/A—uncertain significance
rs37416243722:21,333,927G/A—uncertain significance
rs77769872222:21,334,349C/A—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.