NM_002617.4(PEX10):c.446C>T (p.Thr149Met) AND Peroxisome biogenesis disorder, complementation group 7
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001859699.3
Allele description [Variation Report for NM_002617.4(PEX10):c.446C>T (p.Thr149Met)]
NM_002617.4(PEX10):c.446C>T (p.Thr149Met)
Condition(s)
- Name:
- Peroxisome biogenesis disorder, complementation group 7 (CG7)
- Synonyms:
- Peroxisome biogenesis disorder, complementation group B
- Identifiers:
- MedGen: C1864399
-
Gm7905 predicted pseudogene 7905 [Mus musculus]
Gm7905 predicted pseudogene 7905 [Mus musculus]Gene ID:666045Gene
-
Gm7905 AND (alive[prop]) (1)
Gene
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Last Updated: Sep 29, 2024