NM_024675.4(PALB2):c.1194G>A (p.Val398=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Benign/Likely benign (5 submissions)
- Last evaluated:
- Mar 8, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000127307.24
Allele description [Variation Report for NM_024675.4(PALB2):c.1194G>A (p.Val398=)]
NM_024675.4(PALB2):c.1194G>A (p.Val398=)
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
-
Rattus norvegicus small G protein signaling modulator 3, mRNA (cDNA clone MGC:72...
Rattus norvegicus small G protein signaling modulator 3, mRNA (cDNA clone MGC:72600 IMAGE:5599107), complete cdsgi|38304043|gb|BC062060.1|Nucleotide
-
UI-E-EO0-ahw-k-02-0-UI.r1 UI-E-EO0 Homo sapiens cDNA clone UI-E-EO0-ahw-k-02-0-U...
UI-E-EO0-ahw-k-02-0-UI.r1 UI-E-EO0 Homo sapiens cDNA clone UI-E-EO0-ahw-k-02-0-UI 5', mRNA sequencegi|19042291|gnl|dbEST|11302942|gb|B 09.1|Nucleotide
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Last Updated: Oct 26, 2024