NM_002470.4(MYH3):c.5796+32del AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000252154.5
Allele description [Variation Report for NM_002470.4(MYH3):c.5796+32del]
NM_002470.4(MYH3):c.5796+32del
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
GLI-Kruppel family member GLI1 splice variant, partial [Homo sapiens]
GLI-Kruppel family member GLI1 splice variant, partial [Homo sapiens]gi|538774570|dbj|BAN82437.1|Protein
-
PREDICTED: Homo sapiens protein phosphatase 2 regulatory subunit B'epsilon (PPP2...
PREDICTED: Homo sapiens protein phosphatase 2 regulatory subunit B'epsilon (PPP2R5E), transcript variant X1, mRNAgi|2462540775|ref|XM_054376318.1|Nucleotide
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Last Updated: Mar 10, 2024