NM_001110.4(ADAM10):c.1691A>G (p.Asn564Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002781810.2
Allele description [Variation Report for NM_001110.4(ADAM10):c.1691A>G (p.Asn564Ser)]
NM_001110.4(ADAM10):c.1691A>G (p.Asn564Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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Mus musculus protein tyrosine phosphatase 4a3 (Ptp4a3), transcript variant 12, m...
Mus musculus protein tyrosine phosphatase 4a3 (Ptp4a3), transcript variant 12, mRNAgi|2293430489|ref|NM_001357591.2|Nucleotide
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Homo sapiens adhesion G protein-coupled receptor V1 (ADGRV1), transcript variant...
Homo sapiens adhesion G protein-coupled receptor V1 (ADGRV1), transcript variant 2, non-coding RNAgi|1700447872|ref|NR_003149.2|Nucleotide
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Last Updated: May 1, 2024