PHTF1
putative homeodomain transcription factor 1
Summary
Predicted to be located in cis-Golgi network membrane and endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs762012965 | 1:114,240,913 | T/C | — | uncertain significance |
| rs767404017 | 1:114,240,955 | T/G | — | uncertain significance |
| rs755004020 | 1:114,240,966 | G/T | — | uncertain significance |
| rs758239905 | 1:114,242,357 | T/C | — | uncertain significance |
| rs2524838415 | 1:114,242,385 | T/C | — | uncertain significance |
| rs1221404318 | 1:114,242,391 | G/A | — | uncertain significance |
| rs375148794 | 1:114,243,441 | T/C | — | uncertain significance |
| rs199544296 | 1:114,243,484 | G/A | — | uncertain significance |
| rs578061932 | 1:114,247,302 | G/A | — | uncertain significance |
| rs754290571 | 1:114,247,365 | T/C | — | uncertain significance |
| rs911931113 | 1:114,248,535 | C/T | — | uncertain significance |
| rs1650086013 | 1:114,248,554 | C/A | — | uncertain significance |
| rs1303988199 | 1:114,248,563 | A/C | — | likely benign |
| rs775898880 | 1:114,248,610 | G/A | — | uncertain significance |
| rs145965579 | 1:114,248,625 | C/A | — | uncertain significance |
| rs764311116 | 1:114,248,630 | C/T | — | uncertain significance |
| rs756188876 | 1:114,248,658 | A/C | — | uncertain significance |
| rs757898598 | 1:114,248,681 | C/A | — | uncertain significance |
| rs777185000 | 1:114,248,685 | T/C | — | uncertain significance |
| rs148623704 | 1:114,248,690 | C/T | — | uncertain significance |
| rs199923434 | 1:114,248,693 | A/G | — | uncertain significance |
| rs894797072 | 1:114,248,699 | C/T | — | uncertain significance |
| rs2524901207 | 1:114,248,736 | C/T | — | uncertain significance |
| rs753648508 | 1:114,248,740 | A/T | — | uncertain significance |
| rs755450225 | 1:114,249,334 | A/G | — | uncertain significance |
| rs2524952472 | 1:114,252,992 | C/A | — | uncertain significance |
| rs1156881759 | 1:114,253,078 | C/T | — | uncertain significance |
| rs777369115 | 1:114,254,421 | G/A | — | uncertain significance |
| rs368428698 | 1:114,254,426 | A/G | — | uncertain significance |
| rs773785491 | 1:114,254,445 | T/C | — | uncertain significance |
| rs777041658 | 1:114,254,622 | A/C | — | uncertain significance |
| rs1472612297 | 1:114,254,668 | C/G | — | uncertain significance |
| rs746259493 | 1:114,254,722 | C/T | — | uncertain significance |
| rs529721504 | 1:114,255,919 | A/T | — | uncertain significance |
| rs370038421 | 1:114,255,989 | A/T | — | uncertain significance |
| rs773486132 | 1:114,256,029 | C/T | — | uncertain significance |
| rs1290019914 | 1:114,267,397 | T/A | — | uncertain significance |
| rs769469191 | 1:114,267,398 | C/A | — | uncertain significance |
| rs2525134057 | 1:114,267,412 | C/G | — | uncertain significance |
| rs372900106 | 1:114,267,436 | T/C | — | uncertain significance |
| rs138550041 | 1:114,269,154 | A/C | — | uncertain significance |
| rs35311195 | 1:114,269,155 | T/G | — | uncertain significance |
| rs769238372 | 1:114,280,759 | A/C | — | uncertain significance |
| rs763893990 | 1:114,280,806 | A/C | — | uncertain significance |
| rs146537741 | 1:114,280,839 | C/T | — | uncertain significance |
| rs562492762 | 1:114,280,878 | G/A | — | uncertain significance |
| rs775600933 | 1:114,281,390 | T/A | — | uncertain significance |
| rs1230683 | 1:114,293,247 | A/C | — | — |
| rs766585356 | 1:114,301,304 | C/T | — | uncertain significance |
| rs1159370763 | 1:114,301,313 | C/T | — | uncertain significance |
| rs6679677 | 1:114,303,808 | C/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.