NM_001142966.3(GREB1L):c.74C>T (p.Ser25Phe) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003833031.2
Allele description [Variation Report for NM_001142966.3(GREB1L):c.74C>T (p.Ser25Phe)]
NM_001142966.3(GREB1L):c.74C>T (p.Ser25Phe)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
sp110 nuclear body protein isoform g [Homo sapiens]
sp110 nuclear body protein isoform g [Homo sapiens]gi|1808862655|ref|NP_001365373.1|Protein
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Last Updated: Sep 29, 2024