NM_001355436.2(SPTB):c.6375C>A (p.Asn2125Lys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002793871.2
Allele description [Variation Report for NM_001355436.2(SPTB):c.6375C>A (p.Asn2125Lys)]
NM_001355436.2(SPTB):c.6375C>A (p.Asn2125Lys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Rattus norvegicus 342000077108320 genomic scaffold, whole genome shotgun sequenc...
Rattus norvegicus 342000077108320 genomic scaffold, whole genome shotgun sequencegi|74325628|gnl|WGS:AAHX|3420000771 |gb|CH474034.2|Nucleotide
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Last Updated: May 1, 2024