NM_001366006.2(ADGRL2):c.3790C>A (p.Leu1264Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004223788.1
Allele description [Variation Report for NM_001366006.2(ADGRL2):c.3790C>A (p.Leu1264Met)]
NM_001366006.2(ADGRL2):c.3790C>A (p.Leu1264Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens S100P binding protein (S100PBP), transcript variant X6, ...
PREDICTED: Homo sapiens S100P binding protein (S100PBP), transcript variant X6, mRNAgi|2217270152|ref|XM_047428029.1|Nucleotide
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Last Updated: Nov 3, 2024