NM_030665.4(RAI1):c.796C>T (p.Leu266Phe) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003701895.2
Allele description [Variation Report for NM_030665.4(RAI1):c.796C>T (p.Leu266Phe)]
NM_030665.4(RAI1):c.796C>T (p.Leu266Phe)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens family with sequence similarity 234 member A (FAM234A), ...
PREDICTED: Homo sapiens family with sequence similarity 234 member A (FAM234A), transcript variant X11, mRNAgi|2217307768|ref|XM_017023762.2|Nucleotide
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Last Updated: Sep 29, 2024