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Gene | RET |
Variant | L790X |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | RET L790X indicates any Ret missense mutation that results in replacement of the leucine (L) at amino acid 790 by a different amino acid. |
Associated Drug Resistance | |
Category Variants Paths |
RET mutant RET L790X |
Transcript | NM_020975.6 |
gDNA | chr10:g.43118456_43118458 |
cDNA | c.2368_2370 |
Protein | p.L790 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_020975 | chr10:g.43118456_43118458 | c.2368_2370 | p.L790 | RefSeq | GRCh38/hg38 |
NM_001406744.1 | chr10:g.43118456_43118458 | c.2368_2370 | p.L790 | RefSeq | GRCh38/hg38 |
NM_001406760.1 | chr10:g.43118456_43118458 | c.2368_2370 | p.L790 | RefSeq | GRCh38/hg38 |
NM_001406759.1 | chr10:g.43118456_43118458 | c.2368_2370 | p.L790 | RefSeq | GRCh38/hg38 |
NM_020630.7 | chr10:g.43118456_43118458 | c.2368_2370 | p.L790 | RefSeq | GRCh38/hg38 |
NM_020630 | chr10:g.43118456_43118458 | c.2368_2370 | p.L790 | RefSeq | GRCh38/hg38 |
NM_020630.5 | chr10:g.43118456_43118458 | c.2368_2370 | p.L790 | RefSeq | GRCh38/hg38 |
NM_001406743.1 | chr10:g.43118456_43118458 | c.2368_2370 | p.L790 | RefSeq | GRCh38/hg38 |
NM_020975.5 | chr10:g.43118456_43118458 | c.2368_2370 | p.L790 | RefSeq | GRCh38/hg38 |
NM_020975.6 | chr10:g.43118456_43118458 | c.2368_2370 | p.L790 | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|---|---|---|---|---|---|---|
RET L790X | medullary thyroid carcinoma | not applicable | N/A | Guideline | Risk Factor | Germline RET L790X mutations result in multiple endocrine neoplasia, type 2A (MEN 2A), which is associated with increased risk of developing thyroid medullary carcinoma (NCCN.org). | detail... |