NM_000146.4(FTL):c.*131A>T AND Neuroferritinopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000378331.5
Allele description [Variation Report for NM_000146.4(FTL):c.*131A>T]
NM_000146.4(FTL):c.*131A>T
Condition(s)
-
Homo sapiens cDNA clone IMAGE:3832326, containing frame-shift errors
Homo sapiens cDNA clone IMAGE:3832326, containing frame-shift errorsgi|33871123|gb|BC013880.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Jul 29, 2023