NM_005450.6(NOG):c.396C>A (p.Gly132=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 10, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002177023.5
Allele description [Variation Report for NM_005450.6(NOG):c.396C>A (p.Gly132=)]
NM_005450.6(NOG):c.396C>A (p.Gly132=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens peroxisomal biogenesis factor 5 (PEX5), transcript varia...
PREDICTED: Homo sapiens peroxisomal biogenesis factor 5 (PEX5), transcript variant X8, mRNAgi|2217290277|ref|XM_017019748.2|Nucleotide
-
peroxisomal biogenesis factor 5 isoform X7 [Homo sapiens]
peroxisomal biogenesis factor 5 isoform X7 [Homo sapiens]gi|2217290291|ref|XP_047285224.1|Protein
-
PREDICTED: Homo sapiens peroxisomal biogenesis factor 5 (PEX5), transcript varia...
PREDICTED: Homo sapiens peroxisomal biogenesis factor 5 (PEX5), transcript variant X17, mRNAgi|2217290294|ref|XM_047429270.1|Nucleotide
-
peroxisomal biogenesis factor 5 isoform X12 [Homo sapiens]
peroxisomal biogenesis factor 5 isoform X12 [Homo sapiens]gi|2462533444|ref|XP_054228742.1|Protein
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Last Updated: Feb 28, 2024