NM_138363.3(CEP95):c.1199A>G (p.His400Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004275306.1
Allele description [Variation Report for NM_138363.3(CEP95):c.1199A>G (p.His400Arg)]
NM_138363.3(CEP95):c.1199A>G (p.His400Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024