NM_032730.5(RTN4IP1):c.929G>A (p.Arg310Gln) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003347882.2
Allele description [Variation Report for NM_032730.5(RTN4IP1):c.929G>A (p.Arg310Gln)]
NM_032730.5(RTN4IP1):c.929G>A (p.Arg310Gln)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
nssv2793113 (0)
MeSH
-
nssv2789386 (0)
SRA
-
SAMN37951146 (1)
SRA
-
Motacilla clara torrentium isolate UU_MclaBc66800 NADH dehydrogenase subunit 2 (...
Motacilla clara torrentium isolate UU_MclaBc66800 NADH dehydrogenase subunit 2 (ND2) gene, partial cds; mitochondrialgi|768700459|gb|KP671575.1|Nucleotide
-
cytochrome oxidase subunit 1, partial (mitochondrion) [Ichneumoninae sp. BOLD:AA...
cytochrome oxidase subunit 1, partial (mitochondrion) [Ichneumoninae sp. BOLD:AAM9124]gi|1018225015|gb|AMY42233.1|Protein
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Last Updated: May 1, 2024