NM_024675.4(PALB2):c.1316G>C (p.Gly439Ala) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Dec 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001010937.6
Allele description [Variation Report for NM_024675.4(PALB2):c.1316G>C (p.Gly439Ala)]
NM_024675.4(PALB2):c.1316G>C (p.Gly439Ala)
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
-
high-affinity nickel-transport family protein [Arabidopsis thaliana]
high-affinity nickel-transport family protein [Arabidopsis thaliana]gi|18418571|ref|NP_567976.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 8, 2024