NM_018161.5(NADSYN1):c.508A>C (p.Ile170Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002969715.3
Allele description [Variation Report for NM_018161.5(NADSYN1):c.508A>C (p.Ile170Leu)]
NM_018161.5(NADSYN1):c.508A>C (p.Ile170Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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Homo sapiens protocadherin alpha 1 (PCDHA1), transcript variant 1, mRNA
Homo sapiens protocadherin alpha 1 (PCDHA1), transcript variant 1, mRNAgi|1777535652|ref|NM_018900.4|Nucleotide
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Negative effect of gst-35 on the health span of Caenorhabditis elegans through l...
Negative effect of gst-35 on the health span of Caenorhabditis elegans through lysosomal dysfunction via the pmk-1 and skr genesNegative effect of gst-35 on the health span of Caenorhabditis elegans through lysosomal dysfunction via the pmk-1 and skr genesBioProject
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024