NM_001458.5(FLNC):c.3966C>T (p.Gly1322=) AND not specified
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Aug 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000176382.8
Allele description [Variation Report for NM_001458.5(FLNC):c.3966C>T (p.Gly1322=)]
NM_001458.5(FLNC):c.3966C>T (p.Gly1322=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Causality and Evidence - Adverse Events Associated with Childhood Vaccines
Causality and Evidence - Adverse Events Associated with Childhood Vaccines
-
Mus musculus secretogranin V (Scg5), transcript variant 1, mRNA
Mus musculus secretogranin V (Scg5), transcript variant 1, mRNAgi|2501356916|ref|NM_001420937.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Aug 4, 2024