NM_016139.3(CHCHD2):c.-93C>A AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 11, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002285712.9
Allele description [Variation Report for NM_016139.3(CHCHD2):c.-93C>A]
NM_016139.3(CHCHD2):c.-93C>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
UI-E-EO0-aia-f-13-0-UI.s1 UI-E-EO0 Homo sapiens cDNA clone UI-E-EO0-aia-f-13-0-U...
UI-E-EO0-aia-f-13-0-UI.s1 UI-E-EO0 Homo sapiens cDNA clone UI-E-EO0-aia-f-13-0-UI 3', mRNA sequencegi|18989445|gnl|dbEST|11260482|gb|B 49.1|Nucleotide
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Last Updated: Oct 13, 2024