NM_000475.5(NR0B1):c.16C>A (p.His6Asn) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 18, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002521529.9
Allele description [Variation Report for NM_000475.5(NR0B1):c.16C>A (p.His6Asn)]
NM_000475.5(NR0B1):c.16C>A (p.His6Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
BP688839 Osada Taira anterior neuroectoderm (ANE) pCS105 cDNA library Xenopus la...
BP688839 Osada Taira anterior neuroectoderm (ANE) pCS105 cDNA library Xenopus laevis cDNA clone XL458k01ex 5', mRNA sequencegi|46036794|gnl|dbEST|24553872|dbj| 839.1|Nucleotide
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Last Updated: Oct 20, 2024