NM_000143.4(FH):c.1237-50TC[27] AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002257116.3
Allele description [Variation Report for NM_000143.4(FH):c.1237-50TC[27]]
NM_000143.4(FH):c.1237-50TC[27]
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
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BLOC-2 complex member HPS3 isoform X2 [Homo sapiens]
BLOC-2 complex member HPS3 isoform X2 [Homo sapiens]gi|2462593097|ref|XP_054204067.1|Protein
-
small integral membrane protein 10-like protein 1 isoform 3 [Mus musculus]
small integral membrane protein 10-like protein 1 isoform 3 [Mus musculus]gi|254540194|ref|NP_001156917.1|Protein
-
Salmonella enterica subsp. enterica serovar Arechavaleta strain CFSAN035077, who...
Salmonella enterica subsp. enterica serovar Arechavaleta strain CFSAN035077, whole genome shotgun sequencing projectgi|1808719648|gb|AANYTU000000000.1| U010000000Nucleotide
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golgin subfamily A member 4 isoform X1 [Homo sapiens]
golgin subfamily A member 4 isoform X1 [Homo sapiens]gi|530372318|ref|XP_005265126.1|Protein
-
txid909678[Organism:noexp] (3)
Nucleotide
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Last Updated: May 12, 2024