NM_001909.5(CTSD):c.972+7G>A AND CTSD-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 26, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003957906.1
Allele description [Variation Report for NM_001909.5(CTSD):c.972+7G>A]
NM_001909.5(CTSD):c.972+7G>A
Condition(s)
- Name:
- CTSD-related disorder
- Synonyms:
- CTSD-related condition
- Identifiers:
-
Homo sapiens clone 23771 mRNA sequence
Homo sapiens clone 23771 mRNA sequencegi|2661067|gb|AF035306.1|AF035306Nucleotide
-
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Neurogenic potential of mesenchymal stem cells
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Last Updated: May 26, 2024