NM_001267550.2(TTN):c.66391A>G (p.Thr22131Ala) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 31, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000765558.10
Allele description [Variation Report for NM_001267550.2(TTN):c.66391A>G (p.Thr22131Ala)]
NM_001267550.2(TTN):c.66391A>G (p.Thr22131Ala)
Condition(s)
- Name:
- Dilated cardiomyopathy 1G (CMD1G)
- Identifiers:
- MONDO: MONDO:0011400; MedGen: C1858763; Orphanet: 154; OMIM: 604145
- Name:
- Autosomal recessive limb-girdle muscular dystrophy type 2J (LGMDR10)
- Synonyms:
- Limb-girdle muscular dystrophy, type 2J; MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 10
- Identifiers:
- MONDO: MONDO:0012127; MedGen: C1837342; Orphanet: 140922; OMIM: 608807
- Name:
- Tibial muscular dystrophy (TMD)
- Synonyms:
- Distal myopathy Markesbery-Griggs type; UDD Myopathy; Tibial muscular dystrophy, tardive; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0010870; MedGen: C1838244; Orphanet: 609; OMIM: 600334
- Name:
- Myopathy, myofibrillar, 9, with early respiratory failure (MFM9)
- Synonyms:
- EDSTROM MYOPATHY; MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT; Hereditary myopathy with early respiratory failure; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0011362; MedGen: C1863599; Orphanet: 178464; Orphanet: 34521; OMIM: 603689
Assertion and evidence details
Last Updated: Sep 29, 2024