NM_176824.3(BBS7):c.1234G>T (p.Asp412Tyr) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 11, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002520201.2
Allele description [Variation Report for NM_176824.3(BBS7):c.1234G>T (p.Asp412Tyr)]
NM_176824.3(BBS7):c.1234G>T (p.Asp412Tyr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
eggc.vipgr6 (0)
BioProject
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Last Updated: May 1, 2024