NM_002617.4(PEX10):c.896C>T (p.Ala299Val) AND Peroxisome biogenesis disorder, complementation group 7
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001086392.7
Allele description
NM_002617.4(PEX10):c.896C>T (p.Ala299Val)
Condition(s)
- Name:
- Peroxisome biogenesis disorder, complementation group 7 (CG7)
- Synonyms:
- Peroxisome biogenesis disorder, complementation group B
- Identifiers:
- MedGen: C1864399
-
Homo sapiens semenogelin II (SEMG2), mRNA
Homo sapiens semenogelin II (SEMG2), mRNAgi|4506884|ref|NM_003008.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Aug 4, 2024