NM_000052.7(ATP7A):c.327G>A (p.Lys109=) AND not specified
- Germline classification:
- Benign (4 submissions)
- Last evaluated:
- Mar 31, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000342543.15
Allele description [Variation Report for NM_000052.7(ATP7A):c.327G>A (p.Lys109=)]
NM_000052.7(ATP7A):c.327G>A (p.Lys109=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens cDNA FLJ52270 complete cds, highly similar to Fragile X mental reta...
Homo sapiens cDNA FLJ52270 complete cds, highly similar to Fragile X mental retardation 1 proteingi|194376585|dbj|AK294104.1|Nucleotide
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Last Updated: Sep 16, 2024