NM_001623.5(AIF1):c.196+21G>C AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004122822.1
Allele description [Variation Report for NM_001623.5(AIF1):c.196+21G>C]
NM_001623.5(AIF1):c.196+21G>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024