NM_001267550.2(TTN):c.59926C>T (p.His19976Tyr) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 25, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000474565.4
Allele description [Variation Report for NM_001267550.2(TTN):c.59926C>T (p.His19976Tyr)]
NM_001267550.2(TTN):c.59926C>T (p.His19976Tyr)
Condition(s)
Assertion and evidence details
Last Updated: Nov 30, 2024