NM_001360.3(DHCR7):c.1168C>T (p.His390Tyr) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002332528.2
Allele description [Variation Report for NM_001360.3(DHCR7):c.1168C>T (p.His390Tyr)]
NM_001360.3(DHCR7):c.1168C>T (p.His390Tyr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Slc35b2 solute carrier family 35, member B2 [Mus musculus]
Slc35b2 solute carrier family 35, member B2 [Mus musculus]Gene ID:73836Gene
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Last Updated: Oct 8, 2024