NFIC
nuclear factor I C
Summary
The protein encoded by this gene belongs to the CTF/NF-I family. These are dimeric DNA-binding proteins, and function as cellular transcription factors and as replication factors for adenovirus DNA replication. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs141482719 | 19:3,381,789 | G/A | — | uncertain significance |
| rs2512342512 | 19:3,381,842 | C/T | — | uncertain significance |
| rs769248336 | 19:3,381,962 | A/G | — | uncertain significance |
| rs770764618 | 19:3,381,968 | A/G | — | uncertain significance |
| rs138699938 | 19:3,382,176 | C/T | missense variant | — |
| rs201510675 | 19:3,382,229 | G/C | — | uncertain significance |
| rs776863055 | 19:3,382,233 | G/A | — | uncertain significance |
| rs201011953 | 19:3,382,239 | G/A | — | uncertain significance |
| rs4806932 | 19:3,410,500 | G/C | intron variant | — |
| rs55805295 | 19:3,411,021 | T/C | — | — |
| rs12975645 | 19:3,419,132 | A/C | — | — |
| rs11665658 | 19:3,424,487 | G/C | intron variant | — |
| rs145828739 | 19:3,425,107 | C/A | — | uncertain significance |
| rs7507204 | 19:3,428,834 | G/A | — | — |
| rs771047001 | 19:3,433,519 | C/T | — | uncertain significance |
| rs775927356 | 19:3,433,524 | G/T | — | uncertain significance |
| rs143519997 | 19:3,433,551 | G/A | — | uncertain significance |
| rs755086095 | 19:3,433,563 | G/A | — | uncertain significance |
| rs529235700 | 19:3,434,280 | G/A | — | uncertain significance |
| rs35952068 | 19:3,434,359 | C/G | — | uncertain significance |
| rs762693276 | 19:3,435,087 | G/C | — | uncertain significance |
| rs142790393 | 19:3,435,100 | G/C | — | uncertain significance |
| rs373904141 | 19:3,435,137 | G/A | — | uncertain significance |
| rs773151002 | 19:3,435,193 | G/A | — | uncertain significance |
| rs1469820989 | 19:3,435,196 | A/G | — | uncertain significance |
| rs72974768 | 19:3,435,545 | G/A | regulatory region variant | — |
| rs16991894 | 19:3,437,071 | C/T | — | — |
| rs8105858 | 19:3,438,724 | C/T | — | — |
| rs8106033 | 19:3,440,762 | G/A | intron variant | — |
| rs4807470 | 19:3,443,470 | A/T | intron variant | — |
| rs776854619 | 19:3,449,066 | C/T | — | uncertain significance |
| rs200686979 | 19:3,449,087 | G/A | — | uncertain significance |
| rs755493282 | 19:3,452,638 | G/C | — | uncertain significance |
| rs2512167834 | 19:3,453,768 | G/A | — | uncertain significance |
| rs199528650 | 19:3,453,825 | C/T | — | uncertain significance |
| rs199905745 | 19:3,453,831 | C/T | — | uncertain significance |
| rs774676706 | 19:3,453,843 | G/A | — | uncertain significance |
| rs779544519 | 19:3,453,903 | C/T | — | uncertain significance |
| rs1485134606 | 19:3,456,548 | C/G | — | uncertain significance |
| rs372572344 | 19:3,456,557 | C/G | — | uncertain significance |
| rs376511703 | 19:3,456,580 | C/G | — | uncertain significance |
| rs368331116 | 19:3,456,623 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.