NM_001354604.2(MITF):c.1515C>T (p.Pro505=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 3, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001568941.3
Allele description [Variation Report for NM_001354604.2(MITF):c.1515C>T (p.Pro505=)]
NM_001354604.2(MITF):c.1515C>T (p.Pro505=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024