NM_001083961.2(WDR62):c.3010G>C (p.Ala1004Pro) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003217141.2
Allele description [Variation Report for NM_001083961.2(WDR62):c.3010G>C (p.Ala1004Pro)]
NM_001083961.2(WDR62):c.3010G>C (p.Ala1004Pro)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
SRX24495910 (1)
SRA
-
Licensure
LicensureThe legal authority or formal permission from authorities to carry on certain activities which by law or regulation require such permission. It may be applied to licensure of ...<br/>MeSH
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Last Updated: Sep 1, 2024