NM_001040142.2(SCN2A):c.890A>G (p.Asn297Ser) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001857652.4
Allele description [Variation Report for NM_001040142.2(SCN2A):c.890A>G (p.Asn297Ser)]
NM_001040142.2(SCN2A):c.890A>G (p.Asn297Ser)
Condition(s)
-
BE800884 (0)
MeSH
-
ARHGAP18 [Bos mutus]
ARHGAP18 [Bos mutus]Gene ID:102283538Gene
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Last Updated: Sep 29, 2024