NM_001276345.2(TNNT2):c.294+8G>C AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001963480.5
Allele description [Variation Report for NM_001276345.2(TNNT2):c.294+8G>C]
NM_001276345.2(TNNT2):c.294+8G>C
Condition(s)
- Name:
- Hypertrophic cardiomyopathy 2
- Synonyms:
- Familial hypertrophic cardiomyopathy 2; TNNT2-Related Familial Hypertrophic Cardiomyopathy
- Identifiers:
- MONDO: MONDO:0007266; MedGen: C1861864; OMIM: 115195
-
Homo sapiens lysozyme (LYZ), mRNA
Homo sapiens lysozyme (LYZ), mRNAgi|1732746169|ref|NM_000239.3|Nucleotide
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Last Updated: Sep 16, 2024