NM_006080.3(SEMA3A):c.1954G>A (p.Val652Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003363495.2
Allele description [Variation Report for NM_006080.3(SEMA3A):c.1954G>A (p.Val652Met)]
NM_006080.3(SEMA3A):c.1954G>A (p.Val652Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
cv-d crossveinless d [Drosophila melanogaster]
cv-d crossveinless d [Drosophila melanogaster]Gene ID:41921Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 13, 2024