NM_000546.6(TP53):c.28G>A (p.Val10Ile) AND TP53-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003905099.1
Allele description [Variation Report for NM_000546.6(TP53):c.28G>A (p.Val10Ile)]
NM_000546.6(TP53):c.28G>A (p.Val10Ile)
Condition(s)
- Name:
- TP53-related disorder
- Synonyms:
- TP53-related condition
- Identifiers:
-
Homo sapiens arginyl aminopeptidase (RNPEP), transcript variant 3, mRNA
Homo sapiens arginyl aminopeptidase (RNPEP), transcript variant 3, mRNAgi|1676440197|ref|NM_001319183.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Aug 18, 2024