NM_002617.4(PEX10):c.459T>C (p.Thr153=) AND Peroxisome biogenesis disorder, complementation group 7
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 9, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002894243.2
Allele description [Variation Report for NM_002617.4(PEX10):c.459T>C (p.Thr153=)]
NM_002617.4(PEX10):c.459T>C (p.Thr153=)
Condition(s)
- Name:
- Peroxisome biogenesis disorder, complementation group 7 (CG7)
- Synonyms:
- Peroxisome biogenesis disorder, complementation group B
- Identifiers:
- MedGen: C1864399
-
hypothetical protein [Chlamydia trachomatis]
hypothetical protein [Chlamydia trachomatis]gi|1518798844|ref|WP_123639823.1|Protein
-
hypothetical protein FDI50_gp66 [Enterococcus phage phiSHEF5]
hypothetical protein FDI50_gp66 [Enterococcus phage phiSHEF5]gi|1631935731|ref|YP_009613477.1|Protein
-
sigma-54 dependent transcriptional regulator [Burkholderia stagnalis]
sigma-54 dependent transcriptional regulator [Burkholderia stagnalis]gi|981714102|ref|WP_059908957.1|Protein
-
NF015318 (1)
Protein Family Models
-
cytochrome c oxidase subunit I, partial (mitochondrion) [Morulina sp.]
cytochrome c oxidase subunit I, partial (mitochondrion) [Morulina sp.]gi|2523275184|gb|WJJ40014.1|Protein
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Last Updated: Feb 20, 2024