NM_001286577.2(C2CD3):c.785A>T (p.Asn262Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002555677.2
Allele description [Variation Report for NM_001286577.2(C2CD3):c.785A>T (p.Asn262Ile)]
NM_001286577.2(C2CD3):c.785A>T (p.Asn262Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
mammalian ependymin-related protein 1 isoform 2 precursor [Rattus norvegicus]
mammalian ependymin-related protein 1 isoform 2 precursor [Rattus norvegicus]gi|2207981733|ref|NP_001389366.1|Protein
-
Danio rerio zgc:158305, mRNA (cDNA clone MGC:158305 IMAGE:6969284), complete cds
Danio rerio zgc:158305, mRNA (cDNA clone MGC:158305 IMAGE:6969284), complete cdsgi|120537612|gb|BC129195.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024