NM_001029883.3(PCARE):c.1382T>C (p.Ile461Thr) AND Retinitis pigmentosa
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000298579.5
Allele description [Variation Report for NM_001029883.3(PCARE):c.1382T>C (p.Ile461Thr)]
NM_001029883.3(PCARE):c.1382T>C (p.Ile461Thr)
Condition(s)
-
PHD finger protein 1 isoform b [Homo sapiens]
PHD finger protein 1 isoform b [Homo sapiens]gi|1677537396|ref|NP_077084.2|Protein
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Last Updated: Sep 29, 2024