TFCP2L1
transcription factor CP2 like 1
Summary
Enables RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs34402378 | 2:121,983,657 | C/T | intron variant | — |
| rs34773350 | 2:121,985,759 | C/T | intron variant | — |
| rs74902775 | 2:121,988,391 | C/T | intron variant | — |
| rs11694902 | 2:121,988,884 | G/A | intron variant | — |
| rs528630910 | 2:121,989,430 | G/A | — | uncertain significance |
| rs766101415 | 2:121,989,442 | C/T | — | uncertain significance |
| rs747600759 | 2:121,989,536 | C/T | — | uncertain significance |
| rs35847463 | 2:121,989,657 | G/A | intron variant | — |
| rs147510204 | 2:121,991,705 | T/C | — | uncertain significance |
| rs369690176 | 2:121,992,838 | A/C | — | benign |
| rs13001348 | 2:121,995,065 | G/A | intron variant | — |
| rs777210781 | 2:121,995,243 | C/T | — | uncertain significance |
| rs1405690397 | 2:121,995,246 | T/C | — | uncertain significance |
| rs2468061771 | 2:121,995,266 | C/G | — | uncertain significance |
| rs11689538 | 2:121,995,638 | G/C | regulatory region variant | — |
| rs2468066513 | 2:121,997,158 | G/C | — | uncertain significance |
| rs141932688 | 2:121,997,207 | C/T | — | uncertain significance |
| rs6757766 | 2:121,998,898 | C/T | intron variant | — |
| rs142941586 | 2:121,999,927 | C/T | — | benign |
| rs200414021 | 2:121,999,963 | G/A | — | uncertain significance |
| rs374483735 | 2:122,000,009 | C/G | — | uncertain significance |
| rs267598857 | 2:122,000,012 | G/A | — | uncertain significance |
| rs775901228 | 2:122,004,546 | C/T | — | uncertain significance |
| rs2252862 | 2:122,004,596 | C/A | — | — |
| rs768914903 | 2:122,005,756 | G/A | — | uncertain significance |
| rs199899783 | 2:122,007,191 | G/A | — | uncertain significance |
| rs768363534 | 2:122,007,203 | G/T | — | uncertain significance |
| rs61734658 | 2:122,007,207 | G/A | — | benign |
| rs2713206 | 2:122,007,941 | C/G | — | — |
| rs17006292 | 2:122,018,763 | C/T | — | — |
| rs376149868 | 2:122,038,718 | C/G | — | uncertain significance |
| rs752353544 | 2:122,038,735 | C/T | — | uncertain significance |
| rs1573402593 | 2:122,038,750 | C/G | — | uncertain significance |
| rs1374336174 | 2:122,038,770 | A/G | — | uncertain significance |
| rs1299384312 | 2:122,038,774 | G/A | — | uncertain significance |
| rs36096257 | 2:122,038,783 | G/A | — | benign |
| rs141473122 | 2:122,038,785 | G/T | — | uncertain significance |
| rs1194016225 | 2:122,038,800 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.