NM_001626.6(AKT2):c.821G>A (p.Arg274His) AND not provided
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- May 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003231106.3
Allele description [Variation Report for NM_001626.6(AKT2):c.821G>A (p.Arg274His)]
NM_001626.6(AKT2):c.821G>A (p.Arg274His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens PRAME family member 17 (PRAMEF17), mRNA
Homo sapiens PRAME family member 17 (PRAMEF17), mRNAgi|613410230|ref|NM_001099851.3|Nucleotide
-
ribosomal protein L4 variant, partial [Homo sapiens]
ribosomal protein L4 variant, partial [Homo sapiens]gi|62897675|dbj|BAD96777.1|Protein
-
09p241 - Chromosomal Variation in Man
09p241 - Chromosomal Variation in Man
-
11q130 - Chromosomal Variation in Man
11q130 - Chromosomal Variation in Man
-
Homo sapiens mRNA; cDNA DKFZp434P102 (from clone DKFZp434P102)
Homo sapiens mRNA; cDNA DKFZp434P102 (from clone DKFZp434P102)gi|6807972|emb|AL137419.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 16, 2024