NM_001267550.2(TTN):c.79909G>A (p.Val26637Ile) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 12, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000184863.3
Allele description [Variation Report for NM_001267550.2(TTN):c.79909G>A (p.Val26637Ile)]
NM_001267550.2(TTN):c.79909G>A (p.Val26637Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 29, 2024