NM_017775.4(TTC19):c.184+11C>G AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 23, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002062807.6
Allele description [Variation Report for NM_017775.4(TTC19):c.184+11C>G]
NM_017775.4(TTC19):c.184+11C>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
transcription factor E2F7 [Homo sapiens]
transcription factor E2F7 [Homo sapiens]gi|145580626|ref|NP_976328.2|Protein
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Last Updated: Sep 29, 2024