NM_000257.4(MYH7):c.1283C>A (p.Ala428Asp) AND not provided
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Sep 1, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001093024.21
Allele description [Variation Report for NM_000257.4(MYH7):c.1283C>A (p.Ala428Asp)]
NM_000257.4(MYH7):c.1283C>A (p.Ala428Asp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens DNA replication helicase/nuclease 2 (DNA2), transcript v...
PREDICTED: Homo sapiens DNA replication helicase/nuclease 2 (DNA2), transcript variant X1, mRNAgi|2462517303|ref|XM_054364944.1|Nucleotide
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Last Updated: Oct 8, 2024