NM_002617.4(PEX10):c.912+10del AND Peroxisome biogenesis disorder, complementation group 7
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002157294.5
Allele description [Variation Report for NM_002617.4(PEX10):c.912+10del]
NM_002617.4(PEX10):c.912+10del
Condition(s)
- Name:
- Peroxisome biogenesis disorder, complementation group 7 (CG7)
- Synonyms:
- Peroxisome biogenesis disorder, complementation group B
- Identifiers:
- MedGen: C1864399
-
serine/threonine-protein kinase 38-like isoform X3 [Magallana gigas]
serine/threonine-protein kinase 38-like isoform X3 [Magallana gigas]gi|762098384|ref|XP_011431584.1|Protein
-
uncharacterized protein LACBIDRAFT_381851 [Laccaria bicolor S238N-H82]
uncharacterized protein LACBIDRAFT_381851 [Laccaria bicolor S238N-H82]gi|170089081|ref|XP_001875763.1|Protein
-
Sciaenidae cytochrome oxidase subunit 1 (COI) gene, partial cds; mitochondrial.
Sciaenidae cytochrome oxidase subunit 1 (COI) gene, partial cds; mitochondrial.PopSet: 1189403541PopSet
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024