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| Gene | NRAS |
| Variant | A146X |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | NRAS A146X indicates any NRAS missense mutation that results in replacement of the alanine (A) at amino acid 146 by a different amino acid. |
| Associated Drug Resistance | |
| Category Variants Paths |
NRAS mutant NRAS exon4 NRAS A146X |
| Transcript | NM_002524.5 |
| gDNA | chr1:g.114709581_114709583 |
| cDNA | c.436_438 |
| Protein | p.A146 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_002524.4 | chr1:g.114709581_114709583 | c.436_438 | p.A146 | RefSeq | GRCh38/hg38 |
| NM_002524 | chr1:g.114709581_114709583 | c.436_438 | p.A146 | RefSeq | GRCh38/hg38 |
| NM_002524.5 | chr1:g.114709581_114709583 | c.436_438 | p.A146 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Protein Effect | Treatment Approaches |
|---|---|---|
| NRAS A146X | unknown |