NM_000143.4(FH):c.907T>A (p.Leu303Met) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 13, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002449976.2
Allele description [Variation Report for NM_000143.4(FH):c.907T>A (p.Leu303Met)]
NM_000143.4(FH):c.907T>A (p.Leu303Met)
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
-
NOTO notochord homeobox [Homo sapiens]
NOTO notochord homeobox [Homo sapiens]Gene ID:344022Gene
-
PREDICTED: Homo sapiens nudE neurodevelopment protein 1 (NDE1), transcript varia...
PREDICTED: Homo sapiens nudE neurodevelopment protein 1 (NDE1), transcript variant X5, mRNAgi|2462549450|ref|XM_054380540.1|Nucleotide
-
nuclear distribution protein nudE homolog 1 isoform X9 [Homo sapiens]
nuclear distribution protein nudE homolog 1 isoform X9 [Homo sapiens]gi|2462490675|ref|XP_054185088.1|Protein
-
nuclear distribution protein nudE homolog 1 isoform X17 [Homo sapiens]
nuclear distribution protein nudE homolog 1 isoform X17 [Homo sapiens]gi|2217306418|ref|XP_047290223.1|Protein
-
nuclear distribution protein nudE homolog 1 isoform X1 [Homo sapiens]
nuclear distribution protein nudE homolog 1 isoform X1 [Homo sapiens]gi|530408290|ref|XP_005255453.1|Protein
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Last Updated: May 1, 2024