NM_024675.4(PALB2):c.3029A>C (p.Glu1010Ala) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001018164.4
Allele description [Variation Report for NM_024675.4(PALB2):c.3029A>C (p.Glu1010Ala)]
NM_024675.4(PALB2):c.3029A>C (p.Glu1010Ala)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
Homo sapiens family with sequence similarity 92, member A1, mRNA (cDNA clone IMA...
Homo sapiens family with sequence similarity 92, member A1, mRNA (cDNA clone IMAGE:6514757), partial cdsgi|80479366|gb|BC108707.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024