NM_003079.5(SMARCE1):c.1067A>G (p.Asn356Ser) AND Familial meningioma
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jan 14, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000638926.9
Allele description [Variation Report for NM_003079.5(SMARCE1):c.1067A>G (p.Asn356Ser)]
NM_003079.5(SMARCE1):c.1067A>G (p.Asn356Ser)
Condition(s)
-
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024