NM_004408.4(DNM1):c.474C>T (p.Asp158=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 11, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001662787.9
Allele description [Variation Report for NM_004408.4(DNM1):c.474C>T (p.Asp158=)]
NM_004408.4(DNM1):c.474C>T (p.Asp158=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024