NM_001378615.1(CC2D2A):c.1017+7G>A 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:
- RCV000248826.7
Allele description [Variation Report for NM_001378615.1(CC2D2A):c.1017+7G>A]
NM_001378615.1(CC2D2A):c.1017+7G>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
MULTISPECIES: hypothetical protein [Staphylococcus]
MULTISPECIES: hypothetical protein [Staphylococcus]gi|488416874|ref|WP_002486259.1|Protein
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See more...Assertion and evidence details
Last Updated: Mar 10, 2024