NM_000051.4(ATM):c.7858G>C (p.Val2620Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jun 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001026878.14
Allele description [Variation Report for NM_000051.4(ATM):c.7858G>C (p.Val2620Leu)]
NM_000051.4(ATM):c.7858G>C (p.Val2620Leu)
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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BioProject Links for Protein (Select 1239469427) (2)
BioProject
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Component(Core) Links for Nucleotide (Select 1701264627) (4)
Nucleotide
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SLC1A4 solute carrier family 1 member 4 [Homo sapiens]
SLC1A4 solute carrier family 1 member 4 [Homo sapiens]Gene ID:6509Gene
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Gene Links for GEO Profiles (Select 132637821) (1)
Gene
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Related DataSets for GEO Profiles (Select 58881922) (1)
GEO DataSets
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Last Updated: Sep 8, 2024