NM_001122630.2(CDKN1C):c.881G>A (p.Gly294Asp) AND Beckwith-Wiedemann syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001955909.5
Allele description [Variation Report for NM_001122630.2(CDKN1C):c.881G>A (p.Gly294Asp)]
NM_001122630.2(CDKN1C):c.881G>A (p.Gly294Asp)
Condition(s)
-
C0011860[trait identifier] AND "Gemeinschaftspraxis fuer Humangen... (1)
C0011860[trait identifier] AND "Gemeinschaftspraxis fuer Humangenetik Dresden"[submitter]SearchClinVar
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024