ZNF101
zinc finger protein 101
Summary
Zinc finger proteins (ZNFs), such as ZNF101, bind nucleic acids and perform many key functions, the most important of which is regulating transcription (summary by Bellefroid et al., 1993 [PubMed 8467795]). See ZNF91 (MIM 603971) for general information on ZNFs.[supplied by OMIM, Nov 2010]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs58434384 | 19:19,786,099 | A/G | intron variant | — |
| rs949046289 | 19:19,788,692 | A/G | — | uncertain significance |
| rs371479494 | 19:19,788,729 | G/T | — | uncertain significance |
| rs1375276282 | 19:19,788,762 | T/G | — | uncertain significance |
| rs2304130 | 19:19,789,528 | A/G | splice region variant | — |
| rs137966424 | 19:19,790,114 | G/A | — | uncertain significance |
| rs201804406 | 19:19,790,135 | C/A | — | uncertain significance |
| rs1393092090 | 19:19,790,201 | G/C | — | uncertain significance |
| rs147527039 | 19:19,790,273 | C/T | — | uncertain significance |
| rs746339800 | 19:19,790,292 | G/A | — | uncertain significance |
| rs377049955 | 19:19,790,298 | G/C | — | uncertain significance |
| rs2512768966 | 19:19,790,342 | A/G | — | likely benign |
| rs774598408 | 19:19,790,436 | G/A | — | uncertain significance |
| rs373338300 | 19:19,790,468 | C/T | — | uncertain significance |
| rs201990627 | 19:19,790,528 | G/A | — | uncertain significance |
| rs780496398 | 19:19,790,553 | C/T | — | uncertain significance |
| rs2145060126 | 19:19,790,592 | C/T | — | uncertain significance |
| rs761610943 | 19:19,790,610 | A/G | — | uncertain significance |
| rs527410803 | 19:19,790,627 | G/A | — | uncertain significance |
| rs200382618 | 19:19,790,628 | C/G | — | uncertain significance |
| rs755622740 | 19:19,790,663 | A/G | — | uncertain significance |
| rs1191851304 | 19:19,790,699 | G/C | — | uncertain significance |
| rs1287766281 | 19:19,790,729 | G/A | — | likely benign |
| rs777924760 | 19:19,790,748 | A/G | — | uncertain significance |
| rs375908075 | 19:19,790,808 | C/A | — | uncertain significance |
| rs1311865524 | 19:19,790,865 | A/G | — | uncertain significance |
| rs149729064 | 19:19,791,014 | T/C | — | uncertain significance |
| rs56408111 | 19:19,793,545 | T/C | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.