NM_001267550.2(TTN):c.105468G>A (p.Pro35156=) AND not specified
- Germline classification:
- Benign/Likely benign (8 submissions)
- Last evaluated:
- Nov 8, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000040960.29
Allele description [Variation Report for NM_001267550.2(TTN):c.105468G>A (p.Pro35156=)]
NM_001267550.2(TTN):c.105468G>A (p.Pro35156=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024