NM_015085.5(RAP1GAP2):c.2074G>A (p.Ala692Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004171947.1
Allele description [Variation Report for NM_015085.5(RAP1GAP2):c.2074G>A (p.Ala692Thr)]
NM_015085.5(RAP1GAP2):c.2074G>A (p.Ala692Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Jun 2, 2024