NM_020791.4(TAOK1):c.2467G>T (p.Ala823Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002723362.2
Allele description [Variation Report for NM_020791.4(TAOK1):c.2467G>T (p.Ala823Ser)]
NM_020791.4(TAOK1):c.2467G>T (p.Ala823Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens uncharacterized LOC100128276 (LOC100128276), long non-coding RNA
Homo sapiens uncharacterized LOC100128276 (LOC100128276), long non-coding RNAgi|1236589366|ref|NR_148996.1|Nucleotide
-
Homo sapiens MON1 homolog A, secretory trafficking associated (MON1A), transcrip...
Homo sapiens MON1 homolog A, secretory trafficking associated (MON1A), transcript variant 1, mRNAgi|2020513455|ref|NM_032355.4|Nucleotide
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Last Updated: May 1, 2024