NM_001770.6(CD19):c.1486+9T>A AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002136580.5
Allele description [Variation Report for NM_001770.6(CD19):c.1486+9T>A]
NM_001770.6(CD19):c.1486+9T>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens mRNA for phosphatidic acid phosphatase 2a, complete cds
Homo sapiens mRNA for phosphatidic acid phosphatase 2a, complete cdsgi|2467297|dbj|AB000888.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Mar 5, 2024