NM_000094.4(COL7A1):c.7905C>G (p.Gly2635=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002197930.5
Allele description [Variation Report for NM_000094.4(COL7A1):c.7905C>G (p.Gly2635=)]
NM_000094.4(COL7A1):c.7905C>G (p.Gly2635=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024