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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_020975 | 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_020975.5 | 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_001406765.1 | 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 |
NM_020630.7 | 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_020975.6 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
NM_001406743.1 | 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_020630.5 | chr10:g.43113627_43113629 | c.1831_1833 | p.C611 | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
RET C611X | unknown |