NM_001614.5(ACTG1):c.153C>T (p.Asp51=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002938265.3
Allele description [Variation Report for NM_001614.5(ACTG1):c.153C>T (p.Asp51=)]
NM_001614.5(ACTG1):c.153C>T (p.Asp51=)
Condition(s)
-
LOC127820019 [Homo sapiens]
LOC127820019 [Homo sapiens]Gene ID:127820019Gene
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Last Updated: Sep 29, 2024