NM_001267550.2(TTN):c.14830A>G (p.Thr4944Ala) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 2, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000606245.1
Allele description [Variation Report for NM_001267550.2(TTN):c.14830A>G (p.Thr4944Ala)]
NM_001267550.2(TTN):c.14830A>G (p.Thr4944Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 5, 2022