NAA25
N-alpha-acetyltransferase 25, NatB auxiliary subunit
Summary
This gene encodes the auxiliary subunit of the heteromeric N-terminal acetyltransferase B complex. This complex acetylates methionine residues that are followed by acidic or asparagine residues.[provided by RefSeq, Mar 2010]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1047578 | 12:112,465,129 | A/G | — | — |
| rs11066132 | 12:112,468,206 | C/T | intron variant | — |
| rs79945097 | 12:112,470,241 | G/A | intron variant | — |
| rs779974381 | 12:112,471,092 | T/C | — | uncertain significance |
| rs2078175762 | 12:112,471,152 | A/C | — | uncertain significance |
| rs199692990 | 12:112,471,155 | T/C | — | uncertain significance |
| rs767790120 | 12:112,471,168 | T/A | — | uncertain significance |
| rs764740910 | 12:112,471,188 | G/A | — | likely benign |
| rs12231744 | 12:112,477,055 | T/A | missense variant | — |
| rs920881633 | 12:112,477,063 | T/G | — | uncertain significance |
| rs1197969589 | 12:112,477,073 | T/C | — | uncertain significance |
| rs769148570 | 12:112,477,094 | C/T | — | uncertain significance |
| rs1394905341 | 12:112,478,305 | T/G | — | uncertain significance |
| rs1394962763 | 12:112,479,906 | C/A | — | uncertain significance |
| rs145000175 | 12:112,480,924 | T/C | — | likely benign |
| rs79907395 | 12:112,481,511 | C/T | — | likely benign |
| rs757690276 | 12:112,481,512 | G/A | — | uncertain significance |
| rs765616451 | 12:112,481,535 | G/C | — | uncertain significance |
| rs2543097487 | 12:112,481,583 | C/A | — | uncertain significance |
| rs2543097573 | 12:112,481,628 | G/A | — | uncertain significance |
| rs2543102741 | 12:112,485,558 | G/C | — | uncertain significance |
| rs760779525 | 12:112,486,139 | G/T | — | uncertain significance |
| rs17696736 | 12:112,486,818 | A/G | intron variant | — |
| rs370661609 | 12:112,491,369 | T/C | — | uncertain significance |
| rs781237424 | 12:112,491,395 | G/A | — | likely benign |
| rs2543117689 | 12:112,492,227 | G/C | — | uncertain significance |
| rs2136840548 | 12:112,492,267 | A/G | — | uncertain significance |
| rs781490838 | 12:112,492,319 | G/A | — | uncertain significance |
| rs769717364 | 12:112,492,372 | C/T | — | uncertain significance |
| rs532308916 | 12:112,495,398 | C/T | — | — |
| rs2543131774 | 12:112,499,017 | A/C | — | uncertain significance |
| rs1294751631 | 12:112,499,059 | T/C | — | uncertain significance |
| rs2543131897 | 12:112,499,067 | G/T | — | uncertain significance |
| rs149344901 | 12:112,506,764 | T/C | — | uncertain significance |
| rs771586165 | 12:112,509,782 | C/T | — | uncertain significance |
| rs7298532 | 12:112,510,404 | T/G | — | — |
| rs116873087 | 12:112,511,913 | G/C | downstream gene variant | — |
| rs2078921009 | 12:112,516,025 | C/G | — | uncertain significance |
| rs11066150 | 12:112,518,803 | G/C | — | — |
| rs4767364 | 12:112,521,448 | G/A | intron variant | — |
| rs988419478 | 12:112,528,668 | C/T | — | uncertain significance |
| rs113280084 | 12:112,533,224 | G/C | intron variant | — |
| rs78981331 | 12:112,533,774 | C/T | — | — |
| rs1448900699 | 12:112,546,561 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.