NM_001567.4(INPPL1):c.904C>T (p.Arg302Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003307263.2
Allele description [Variation Report for NM_001567.4(INPPL1):c.904C>T (p.Arg302Cys)]
NM_001567.4(INPPL1):c.904C>T (p.Arg302Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
PREDICTED: Homo sapiens NSF attachment protein beta (NAPB), transcript variant X...
PREDICTED: Homo sapiens NSF attachment protein beta (NAPB), transcript variant X5, mRNAgi|2462581126|ref|XM_054323809.1|Nucleotide
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Last Updated: May 1, 2024