NM_001267550.2(TTN):c.100459C>T (p.Pro33487Ser) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Feb 4, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001811300.14
Allele description [Variation Report for NM_001267550.2(TTN):c.100459C>T (p.Pro33487Ser)]
NM_001267550.2(TTN):c.100459C>T (p.Pro33487Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Nov 24, 2024