NM_000053.4(ATP7B):c.1168A>G (p.Ile390Val) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 11, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002327425.2
Allele description [Variation Report for NM_000053.4(ATP7B):c.1168A>G (p.Ile390Val)]
NM_000053.4(ATP7B):c.1168A>G (p.Ile390Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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Halomonas sp. strain ESSAA1Glu 4C 16S ribosomal RNA gene, partial sequence
Halomonas sp. strain ESSAA1Glu 4C 16S ribosomal RNA gene, partial sequencegi|1239807581|gb|MF804952.1|Nucleotide
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Senecio douglasii internal transcribed spacer 1, partial sequence
Senecio douglasii internal transcribed spacer 1, partial sequencegi|8132477|gb|AF161640.1|Nucleotide
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PREDICTED: Homo sapiens ankyrin repeat domain 65 (ANKRD65), transcript variant X...
PREDICTED: Homo sapiens ankyrin repeat domain 65 (ANKRD65), transcript variant X1, mRNAgi|2217267601|ref|XM_005244752.5|Nucleotide
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Last Updated: Oct 8, 2024