PHF14
PHD finger protein 14
Summary
Enables histone binding activity. Predicted to be involved in several processes, including germinal center B cell differentiation; lung development; and negative regulation of mesenchymal cell proliferation involved in lung development. Located in chromatin; cytoplasm; and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs750253833 | 7:11,014,477 | A/G | — | uncertain significance |
| rs2534121549 | 7:11,022,020 | G/T | — | uncertain significance |
| rs2534121673 | 7:11,022,047 | G/C | — | uncertain significance |
| rs767770715 | 7:11,022,245 | A/G | — | uncertain significance |
| rs988712186 | 7:11,022,329 | C/T | — | uncertain significance |
| rs1314587279 | 7:11,022,362 | C/G | — | uncertain significance |
| rs374664759 | 7:11,022,397 | A/G | — | uncertain significance |
| rs2534123543 | 7:11,022,398 | C/T | — | uncertain significance |
| rs781174027 | 7:11,022,400 | G/A | — | likely benign |
| rs201923929 | 7:11,022,455 | C/G | — | uncertain significance |
| rs376684531 | 7:11,022,552 | A/C | — | uncertain significance |
| rs1166378479 | 7:11,022,589 | G/C | — | uncertain significance |
| rs749980412 | 7:11,022,650 | A/T | — | uncertain significance |
| rs2534124782 | 7:11,022,657 | A/T | — | uncertain significance |
| rs1394297119 | 7:11,022,659 | A/C | — | uncertain significance |
| rs747207586 | 7:11,022,685 | G/T | — | uncertain significance |
| rs754076838 | 7:11,030,369 | C/A | — | uncertain significance |
| rs370005938 | 7:11,030,372 | A/C | — | uncertain significance |
| rs2128310303 | 7:11,030,393 | T/G | — | uncertain significance |
| rs1782423439 | 7:11,030,470 | T/A | — | uncertain significance |
| rs2533645485 | 7:11,053,430 | T/A | — | uncertain significance |
| rs929943899 | 7:11,053,469 | G/A | — | uncertain significance |
| rs2533645632 | 7:11,053,523 | G/C | — | uncertain significance |
| rs183600932 | 7:11,058,396 | C/T | intron variant | — |
| rs984685706 | 7:11,062,584 | A/G | — | uncertain significance |
| rs1469223527 | 7:11,068,315 | G/C | — | uncertain significance |
| rs2533676966 | 7:11,068,326 | G/T | — | uncertain significance |
| rs140828362 | 7:11,068,409 | A/G | — | likely benign |
| rs746336846 | 7:11,076,090 | C/G | — | uncertain significance |
| rs2533694360 | 7:11,076,111 | C/T | — | likely benign |
| rs1316732849 | 7:11,078,432 | C/G | — | uncertain significance |
| rs771805157 | 7:11,080,308 | A/G | — | uncertain significance |
| rs201677864 | 7:11,091,394 | C/T | — | uncertain significance |
| rs2533762079 | 7:11,101,460 | A/C | — | uncertain significance |
| rs747850121 | 7:11,101,700 | A/C | — | uncertain significance |
| rs2995903 | 7:11,124,528 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.