NM_000264.5(PTCH1):c.3384T>C (p.Asp1128=) AND Gorlin syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 23, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002204479.6
Allele description [Variation Report for NM_000264.5(PTCH1):c.3384T>C (p.Asp1128=)]
NM_000264.5(PTCH1):c.3384T>C (p.Asp1128=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024