NM_001110.4(ADAM10):c.2200C>A (p.Arg734Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003265219.2
Allele description [Variation Report for NM_001110.4(ADAM10):c.2200C>A (p.Arg734Ser)]
NM_001110.4(ADAM10):c.2200C>A (p.Arg734Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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PREDICTED: Mus musculus PHD finger protein 12 (Phf12), transcript variant X4, mR...
PREDICTED: Mus musculus PHD finger protein 12 (Phf12), transcript variant X4, mRNAgi|1720366209|ref|XM_030246034.1|Nucleotide
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Taxonomy Links for Protein (Select 148689054) (1)
Taxonomy
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Last Updated: May 1, 2024