NM_001098.3(ACO2):c.2036G>A (p.Arg679His) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Sep 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002958883.3
Allele description [Variation Report for NM_001098.3(ACO2):c.2036G>A (p.Arg679His)]
NM_001098.3(ACO2):c.2036G>A (p.Arg679His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens placental protein 25 variant (PP25) mRNA, complete cds
Homo sapiens placental protein 25 variant (PP25) mRNA, complete cdsgi|33311832|gb|AF417114.1|Nucleotide
-
Homo sapiens mRNA; cDNA DKFZp686F1544 (from clone DKFZp686F1544); complete cds
Homo sapiens mRNA; cDNA DKFZp686F1544 (from clone DKFZp686F1544); complete cdsgi|31874680|emb|BX538213.1|Nucleotide
-
Homo sapiens BTRCP2 mRNA for F-box and WD-repeats protein beta-TRCP2 isoform A, ...
Homo sapiens BTRCP2 mRNA for F-box and WD-repeats protein beta-TRCP2 isoform A, complete cdsgi|7209808|dbj|AB033279.1|Nucleotide
-
PREDICTED: Homo sapiens solute carrier family 25 member 35 (SLC25A35), transcrip...
PREDICTED: Homo sapiens solute carrier family 25 member 35 (SLC25A35), transcript variant X4, mRNAgi|2462555205|ref|XM_054316090.1|Nucleotide
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Last Updated: Sep 1, 2024