FAM53A
family with sequence similarity 53 member A
Summary
Predicted to be involved in protein import into nucleus. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs778363690 | 4:1,643,046 | C/T | — | uncertain significance |
| rs565614356 | 4:1,643,058 | G/A | — | uncertain significance |
| rs779785935 | 4:1,643,073 | C/T | — | likely benign |
| rs199624823 | 4:1,643,085 | C/T | — | uncertain significance |
| rs139732204 | 4:1,643,115 | T/C | — | uncertain significance |
| rs202151764 | 4:1,643,123 | C/T | — | uncertain significance |
| rs566928749 | 4:1,643,124 | G/A | — | uncertain significance |
| rs1205654645 | 4:1,643,166 | T/G | — | uncertain significance |
| rs527699371 | 4:1,643,190 | G/A | — | uncertain significance |
| rs2546509652 | 4:1,643,192 | C/A | — | uncertain significance |
| rs748109680 | 4:1,643,213 | A/G | — | likely benign |
| rs1422086559 | 4:1,643,271 | G/A | — | uncertain significance |
| rs2546510742 | 4:1,643,328 | T/G | — | uncertain significance |
| rs543282682 | 4:1,644,990 | A/T | — | — |
| rs371975302 | 4:1,656,737 | G/A | — | uncertain significance |
| rs750685582 | 4:1,656,748 | G/A | — | uncertain significance |
| rs116661726 | 4:1,656,760 | C/T | — | benign |
| rs762709666 | 4:1,656,761 | G/A | — | uncertain significance |
| rs376520001 | 4:1,656,773 | G/A | — | uncertain significance |
| rs142856177 | 4:1,656,776 | G/C | — | benign |
| rs922444594 | 4:1,656,781 | C/T | — | likely benign |
| rs766673560 | 4:1,656,797 | C/A | — | uncertain significance |
| rs112026417 | 4:1,656,822 | C/G | — | benign |
| rs115046452 | 4:1,656,824 | G/A | — | benign |
| rs200357652 | 4:1,656,836 | C/A | — | uncertain significance |
| rs115785763 | 4:1,656,856 | G/A | — | benign |
| rs201035222 | 4:1,656,883 | G/C | — | benign |
| rs182903545 | 4:1,656,888 | G/T | — | likely benign |
| rs370251492 | 4:1,656,925 | C/T | — | uncertain significance |
| rs367598214 | 4:1,656,957 | G/A | — | benign |
| rs752191120 | 4:1,656,992 | C/T | — | uncertain significance |
| rs565628128 | 4:1,657,039 | G/A | missense variant | — |
| rs892669659 | 4:1,657,040 | C/T | — | uncertain significance |
| rs749267709 | 4:1,657,088 | C/T | — | uncertain significance |
| rs753341886 | 4:1,657,091 | C/T | — | uncertain significance |
| rs1272899670 | 4:1,657,124 | T/C | — | uncertain significance |
| rs570727471 | 4:1,657,127 | C/T | — | likely benign |
| rs761377314 | 4:1,657,186 | C/G | — | uncertain significance |
| rs1168570310 | 4:1,657,192 | C/T | — | uncertain significance |
| rs371772875 | 4:1,657,203 | C/T | — | benign |
| rs778853792 | 4:1,657,208 | G/A | — | uncertain significance |
| rs369257679 | 4:1,657,223 | G/A | — | uncertain significance |
| rs764345958 | 4:1,657,255 | G/A | — | uncertain significance |
| rs1182069438 | 4:1,657,357 | G/A | — | uncertain significance |
| rs747554055 | 4:1,657,381 | A/C | — | uncertain significance |
| rs368575496 | 4:1,657,387 | G/A | — | uncertain significance |
| rs762299168 | 4:1,657,388 | G/A | — | uncertain significance |
| rs79448086 | 4:1,659,137 | T/C | — | benign |
| rs545677074 | 4:1,659,159 | G/A | — | uncertain significance |
| rs751076162 | 4:1,659,190 | C/A | — | uncertain significance |
| rs13129308 | 4:1,683,026 | T/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.