TCF19
transcription factor 19
Summary
This gene encodes a protein that contains a PHD-type zinc finger domain and likely functions as a transcription factor. The encoded protein plays a role proliferation and apoptosis of pancreatic beta cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3130453 | 6:31,124,849 | C/T | stop gained | — |
| rs17190769 | 6:31,127,037 | C/A | — | — |
| rs762258908 | 6:31,127,316 | C/A | — | uncertain significance |
| rs778295498 | 6:31,127,374 | C/A | — | uncertain significance |
| rs2533169150 | 6:31,127,440 | G/A | — | likely benign |
| rs763067666 | 6:31,127,442 | G/A | — | uncertain significance |
| rs755855284 | 6:31,127,455 | G/T | — | uncertain significance |
| rs9263789 | 6:31,128,329 | G/A | downstream gene variant | — |
| rs3130934 | 6:31,128,552 | A/C | downstream gene variant | — |
| rs144374591 | 6:31,129,263 | G/A | — | uncertain significance |
| rs201756282 | 6:31,129,265 | C/A | — | uncertain significance |
| rs899519362 | 6:31,129,293 | C/A | — | uncertain significance |
| rs7750641 | 6:31,129,310 | C/T | — | benign |
| rs749526101 | 6:31,129,329 | C/T | — | uncertain significance |
| rs1161644010 | 6:31,129,418 | G/A | — | uncertain significance |
| rs779159917 | 6:31,129,467 | G/A | — | uncertain significance |
| rs188298136 | 6:31,129,542 | G/A | — | benign |
| rs767070147 | 6:31,129,568 | A/C | — | uncertain significance |
| rs1487939684 | 6:31,129,607 | C/T | — | uncertain significance |
| rs2073721 | 6:31,129,616 | A/G | — | benign |
| rs773718194 | 6:31,129,647 | G/A | — | uncertain significance |
| rs2073724 | 6:31,129,707 | C/G | missense variant | — |
| rs541001159 | 6:31,129,739 | A/G | — | uncertain significance |
| rs371901587 | 6:31,130,274 | G/A | — | uncertain significance |
| rs1422412321 | 6:31,130,297 | A/G | — | uncertain significance |
| rs536786193 | 6:31,130,321 | G/A | — | uncertain significance |
| rs762319085 | 6:31,130,399 | G/A | — | likely benign |
| rs1193959925 | 6:31,130,415 | C/T | — | uncertain significance |
| rs1419881 | 6:31,130,593 | G/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.