NM_001267550.2(TTN):c.74763C>T (p.Ser24921=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 5, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000592268.3
Allele description
NM_001267550.2(TTN):c.74763C>T (p.Ser24921=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 16, 2021