CHURC1-FNTB
CHURC1-FNTB readthrough
Summary
This locus represents naturally occurring read-through transcription between the neighboring CHURC1 (churchill domain containing 1) and FNTB (farnesyltransferase, CAAX box, beta) on chromosome 14. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Feb 2011]
Known Variants3 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7161378 | 14:65,450,780 | T/C | regulatory region variant | — |
| rs56118026 | 14:65,479,115 | C/A | — | benign |
| rs200759729 | 14:65,499,312 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.