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Gene | RET |
Variant | Y791X |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | RET Y791X indicates any Ret missense mutation that results in replacement of the tyrosine (Y) at amino acid 791 by a different amino acid. |
Associated Drug Resistance | |
Category Variants Paths |
RET mutant RET Y791X |
Transcript | NM_020975.6 |
gDNA | chr10:g.43118459_43118461 |
cDNA | c.2371_2373 |
Protein | p.Y791 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001406744.1 | chr10:g.43118459_43118461 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
NM_020975.5 | chr10:g.43118459_43118461 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
NM_020975.6 | chr10:g.43118459_43118461 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
NM_001406780.1 | chr10:g.43128192_43128194 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
NM_001406759.1 | chr10:g.43118459_43118461 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
NM_020630 | chr10:g.43118459_43118461 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
NM_020630.7 | chr10:g.43118459_43118461 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
NM_001406760.1 | chr10:g.43118459_43118461 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
NM_020975 | chr10:g.43118459_43118461 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
NM_001406743.1 | chr10:g.43118459_43118461 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
NM_001406779.1 | chr10:g.43128192_43128194 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
NM_020630.5 | chr10:g.43118459_43118461 | c.2371_2373 | p.Y791 | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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