NM_001267550.2(TTN):c.36391C>T (p.Arg12131Cys) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 31, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000474800.5
Allele description [Variation Report for NM_001267550.2(TTN):c.36391C>T (p.Arg12131Cys)]
NM_001267550.2(TTN):c.36391C>T (p.Arg12131Cys)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024