NM_016940.3(RWDD2B):c.773A>G (p.Asp258Gly) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004447101.1
Allele description [Variation Report for NM_016940.3(RWDD2B):c.773A>G (p.Asp258Gly)]
NM_016940.3(RWDD2B):c.773A>G (p.Asp258Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: May 7, 2024