NM_001458.5(FLNC):c.1813+2T>C AND not provided
- Germline classification:
- Pathogenic (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001529273.4
Allele description [Variation Report for NM_001458.5(FLNC):c.1813+2T>C]
NM_001458.5(FLNC):c.1813+2T>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
BioProject Links for Nucleotide (Select 2217312515) (1)
BioProject
-
PREDICTED: Homo sapiens phospholipase D2 (PLD2), transcript variant X1, mRNA
PREDICTED: Homo sapiens phospholipase D2 (PLD2), transcript variant X1, mRNAgi|2462556056|ref|XM_054316508.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023