NM_000258.3(MYL3):c.435T>C (p.Asn145=) AND Cardiomyopathy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 2, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001182315.2
Allele description [Variation Report for NM_000258.3(MYL3):c.435T>C (p.Asn145=)]
NM_000258.3(MYL3):c.435T>C (p.Asn145=)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
-
protocadherin-7 isoform X10 [Mus musculus]
protocadherin-7 isoform X10 [Mus musculus]gi|568934371|ref|XP_006504091.1|Protein
-
PREDICTED: Mus musculus protocadherin 7 (Pcdh7), transcript variant X8, mRNA
PREDICTED: Mus musculus protocadherin 7 (Pcdh7), transcript variant X8, mRNAgi|1907164946|ref|XM_036165309.1|Nucleotide
-
PREDICTED: Mus musculus protocadherin 7 (Pcdh7), transcript variant X5, mRNA
PREDICTED: Mus musculus protocadherin 7 (Pcdh7), transcript variant X5, mRNAgi|1720414301|ref|XM_006504023.4|Nucleotide
-
D-amino acid oxidase regulator isoform 3 [Homo sapiens]
D-amino acid oxidase regulator isoform 3 [Homo sapiens]gi|240120029|ref|NP_001155286.1|Protein
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Last Updated: Sep 29, 2024