NM_000546.6(TP53):c.38C>T (p.Pro13Leu) AND Adrenocortical carcinoma, hereditary
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003469151.1
Allele description [Variation Report for NM_000546.6(TP53):c.38C>T (p.Pro13Leu)]
NM_000546.6(TP53):c.38C>T (p.Pro13Leu)
Condition(s)
-
Homo sapiens nuclear receptor corepressor 1 (NCOR1), RefSeqGene on chromosome 17
Homo sapiens nuclear receptor corepressor 1 (NCOR1), RefSeqGene on chromosome 17gi|1027250631|ref|NG_047111.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024