NM_000391.4(TPP1):c.381-2A>G AND not provided
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Jul 21, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001860125.3
Allele description [Variation Report for NM_000391.4(TPP1):c.381-2A>G]
NM_000391.4(TPP1):c.381-2A>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens CCR4-NOT transcription complex subunit 6 (CNOT6), transcript varian...
Homo sapiens CCR4-NOT transcription complex subunit 6 (CNOT6), transcript variant 3, mRNAgi|1635381372|ref|NM_001370474.1|Nucleotide
-
Homo sapiens cDNA clone IMAGE:30418449
Homo sapiens cDNA clone IMAGE:30418449gi|60551989|gb|BC090918.1|Nucleotide
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Last Updated: Feb 14, 2024