NM_001267550.2(TTN):c.34307A>G (p.Lys11436Arg) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Nov 12, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001289367.4
Allele description [Variation Report for NM_001267550.2(TTN):c.34307A>G (p.Lys11436Arg)]
NM_001267550.2(TTN):c.34307A>G (p.Lys11436Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024