NM_001458.5(FLNC):c.850+18G>A AND not specified
- Germline classification:
- Benign (5 submissions)
- Last evaluated:
- Apr 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000252828.11
Allele description [Variation Report for NM_001458.5(FLNC):c.850+18G>A]
NM_001458.5(FLNC):c.850+18G>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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C2675237[conceptid] (1)
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Mitochondrial trifunctional protein deficiency
Mitochondrial trifunctional protein deficiencyMedGen
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C1969443[conceptid] (1)
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uncharacterized protein LOC100250913 isoform X1 [Vitis vinifera]
uncharacterized protein LOC100250913 isoform X1 [Vitis vinifera]gi|359472808|ref|XP_002274465.2|Protein
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See more...Assertion and evidence details
Last Updated: Mar 10, 2024