NM_000430.4(PAFAH1B1):c.608A>G (p.Asn203Ser) AND Lissencephaly due to LIS1 mutation
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002489971.1
Allele description [Variation Report for NM_000430.4(PAFAH1B1):c.608A>G (p.Asn203Ser)]
NM_000430.4(PAFAH1B1):c.608A>G (p.Asn203Ser)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024