NAA15

N-alpha-acetyltransferase 15, NatA auxiliary subunit

Summary

N-alpha-acetylation is among the most common post-translational protein modifications in eukaryotic cells. This process involves the transfer of an acetyl group from acetyl-coenzyme A to the alpha-amino group on a nascent polypeptide and is essential for normal cell function. This gene encodes the auxillary subunit of the N-terminal acetyltransferase A (NatA) complex. [provided by RefSeq, Jan 2017]

Known Variants305 total

rsidPosition (GRCh37)AllelesClassClinVar
rs38067664:140,222,371G/A—benign
rs68519544:140,222,480T/C—benign
rs38067654:140,222,537A/G—benign
rs25302593564:140,222,951C/T—uncertain significance
rs21108006994:140,222,956A/G—uncertain significance
rs25302594194:140,222,959G/T—pathogenic
rs21108008534:140,222,977C/G—likely pathogenic
rs2013928044:140,223,001C/T—benign
rs1893505934:140,243,320A/Gregulatory region variant—
rs21108884034:140,252,465G/C—uncertain significance
rs2005253904:140,255,311C/G—benign
rs13289949534:140,255,318G/A—likely benign
rs25303515364:140,255,326A/C—likely pathogenic
rs1998857474:140,255,345A/G—likely benign
rs25303515754:140,255,348G/A—likely benign
rs17471227714:140,255,358G/T—pathogenic
rs25303516104:140,255,371G/A—uncertain significance
rs15791016974:140,255,376C/T—pathogenic
rs25303516274:140,255,378A/G—likely benign
rs21108959654:140,255,407A/G—conflicting classifications of pathogenicity
rs7581512544:140,255,419G/A—likely benign
rs1995527014:140,255,428T/A—benign
rs7643283564:140,258,005C/A—uncertain significance
rs7621337974:140,258,028T/C—likely benign
rs14480269884:140,258,044A/G—uncertain significance
rs25303579074:140,258,056C/T—uncertain significance
rs12363090744:140,258,070C/T—uncertain significance
rs17472184844:140,258,071G/A—uncertain significance
rs21109020084:140,258,080T/C—likely pathogenic
rs14040762074:140,258,081G/T—likely pathogenic
rs7662725264:140,258,087T/C—uncertain significance
rs3687808024:140,258,093G/A—uncertain significance
rs17472194774:140,258,095A/G—uncertain significance
rs15791066854:140,262,046C/T—likely benign
rs25303685004:140,262,066G/A—uncertain significance
rs7476016314:140,262,067T/C—likely benign
rs7685861404:140,262,073C/T—likely benign
rs7768372474:140,262,079T/C—likely benign
rs17473639324:140,262,081G/A—uncertain significance
rs572693594:140,262,082C/A—benign
rs15609651644:140,262,087T/C—conflicting classifications of pathogenicity
rs21109110054:140,262,101A/T—pathogenic
rs25303686564:140,262,130C/G—pathogenic
rs25303686954:140,262,147G/A—pathogenic
rs21109110544:140,262,148G/A—likely pathogenic
rs8895430974:140,262,155G/A—pathogenic
rs25303687244:140,262,159A/G—conflicting classifications of pathogenicity
rs3719856064:140,262,190A/G—likely benign
rs12746334984:140,262,203C/T—pathogenic
rs25303688714:140,262,215G/A—uncertain significance
rs25303688784:140,262,221A/C—likely benign
rs7635029584:140,262,241T/G—likely benign
rs119444344:140,263,849G/A—benign
rs25303751624:140,263,973T/C—likely benign
rs21109152384:140,263,979G/A—likely pathogenic
rs7735882034:140,263,988G/A—likely benign
rs9852311554:140,263,991T/C—likely benign
rs21109152994:140,264,003G/T—uncertain significance
rs15609660864:140,264,007C/T—pathogenic
rs7754170234:140,264,015G/A—likely benign
rs3688171724:140,264,024A/G—likely benign
rs25303753244:140,264,041C/G—uncertain significance
rs21109153644:140,264,052C/T—uncertain significance
rs13265056884:140,264,053A/G—uncertain significance
rs25303754004:140,264,059T/A—pathogenic
rs25303754624:140,264,082A/G—uncertain significance
rs7581133544:140,264,099T/C—likely benign
rs25303755034:140,264,110A/C—uncertain significance
rs7802692234:140,264,124A/G—likely benign
rs3765624934:140,264,131A/G—likely benign
rs727265164:140,264,421T/C—benign
rs68489504:140,264,431T/G—benign
rs1160342074:140,265,237G/A—benign
rs779686454:140,265,241G/A—benign
rs25303787474:140,265,327T/A—likely benign
rs7499918864:140,265,332A/G—likely benign
rs13767366374:140,265,345C/G—likely benign
rs25303788764:140,265,347C/T—uncertain significance
rs3738625434:140,265,351C/T—benign
rs15609668064:140,265,371G/A—uncertain significance
rs25303790124:140,265,394C/G—uncertain significance
rs10155353184:140,265,403C/T—uncertain significance
rs7493885004:140,265,404G/A—uncertain significance
rs13607133324:140,265,412G/T—uncertain significance
rs2000185474:140,265,415C/T—likely benign
rs25303791564:140,265,443G/T—uncertain significance
rs25303791814:140,265,457C/T—likely pathogenic
rs15791095654:140,265,494G/A—pathogenic
rs131469444:140,265,621G/A—benign
rs21225934:140,265,631A/G—benign
rs13329923064:140,270,611A/G—uncertain significance
rs14295912094:140,270,625T/A—uncertain significance
rs14647958564:140,270,630C/A—uncertain significance
rs25303915704:140,270,632A/G—uncertain significance
rs340544524:140,270,635A/G—benign
rs3704325374:140,270,640G/A—conflicting classifications of pathogenicity
rs25303916084:140,270,645G/T—pathogenic
rs10024021014:140,270,659T/A—uncertain significance
rs17477104804:140,270,663T/G—uncertain significance
rs15791137794:140,270,667G/A—uncertain significance

Showing 100 of 305 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.