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| Gene | RET |
| Variant | C611X |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | RET C611X indicates any Ret missense mutation that results in replacement of the cysteine (C) at amino acid 611 by a different amino acid. |
| Associated Drug Resistance | |
| Category Variants Paths |
RET mutant RET C611X |
| Transcript | NM_020975.6 |
| gDNA | chr10:g.43113627_43113629 |
| cDNA | c.1831_1833 |
| Protein | p.C611 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001406743.1 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| NM_001406765.1 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| NM_001406763.1 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| NM_020975 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| NM_020630.5 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| NM_020975.5 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| NM_001406760.1 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| NM_020630.7 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| NM_020630 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| NM_020975.6 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| NM_001406744.1 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| NM_001406759.1 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
| Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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