NM_021151.4(CROT):c.1352G>A (p.Arg451His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 23, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004239938.1
Allele description [Variation Report for NM_021151.4(CROT):c.1352G>A (p.Arg451His)]
NM_021151.4(CROT):c.1352G>A (p.Arg451His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens isolate CHM13 chromosome 19, alternate assembly T2T-CHM13v2.0
Homo sapiens isolate CHM13 chromosome 19, alternate assembly T2T-CHM13v2.0gi|2194972797|gnl|ASM:GCF_009914825 ef|NC_060943.1||gpp|GPC_000012758.1||gnl|NCBI_GENOMES|119579Nucleotide
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Last Updated: Jun 2, 2024