NM_021954.4(GJA3):c.245T>A (p.Ile82Asn) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002788669.2
Allele description [Variation Report for NM_021954.4(GJA3):c.245T>A (p.Ile82Asn)]
NM_021954.4(GJA3):c.245T>A (p.Ile82Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens cDNA FLJ20021 fis, clone ADSE01233
Homo sapiens cDNA FLJ20021 fis, clone ADSE01233gi|7019844|dbj|AK000028.1|Nucleotide
-
LOC123477795 [Homo sapiens]
LOC123477795 [Homo sapiens]Gene ID:123477795Gene
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Last Updated: May 1, 2024