NM_144573.4(NEXN):c.1366G>A (p.Gly456Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 30, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000041158.5
Allele description [Variation Report for NM_144573.4(NEXN):c.1366G>A (p.Gly456Arg)]
NM_144573.4(NEXN):c.1366G>A (p.Gly456Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
large ribosomal subunit protein uL3 isoform a [Homo sapiens]
large ribosomal subunit protein uL3 isoform a [Homo sapiens]gi|4506649|ref|NP_000958.1|Protein
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Last Updated: Mar 5, 2024