NM_000257.4(MYH7):c.4326G>A (p.Leu1442=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 3, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000151239.4
Allele description [Variation Report for NM_000257.4(MYH7):c.4326G>A (p.Leu1442=)]
NM_000257.4(MYH7):c.4326G>A (p.Leu1442=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
LOC100132077 [Homo sapiens]
LOC100132077 [Homo sapiens]Gene ID:100132077Gene
-
100132077[uid] AND (alive[prop]) (1)
Gene
-
PPX1 [Saccharomyces cerevisiae S288C]
PPX1 [Saccharomyces cerevisiae S288C]Gene ID:856608Gene
-
856608[uid] AND (alive[prop]) (1)
Gene
-
TCEAL3 AND (alive[prop]) (158)
Gene
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Last Updated: May 7, 2024