NM_001267550.2(TTN):c.17437T>A (p.Cys5813Ser) AND not provided
- Germline classification:
- Uncertain significance (3 submissions)
- Last evaluated:
- Jul 29, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001699930.6
Allele description [Variation Report for NM_001267550.2(TTN):c.17437T>A (p.Cys5813Ser)]
NM_001267550.2(TTN):c.17437T>A (p.Cys5813Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024