NM_001080414.4(CCDC88C):c.5906C>T (p.Pro1969Leu) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002542032.3
Allele description [Variation Report for NM_001080414.4(CCDC88C):c.5906C>T (p.Pro1969Leu)]
NM_001080414.4(CCDC88C):c.5906C>T (p.Pro1969Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens R3H domain containing 2 (R3HDM2), transcript variant 3, mRNA
Homo sapiens R3H domain containing 2 (R3HDM2), transcript variant 3, mRNAgi|1677539361|ref|NM_014925.5|Nucleotide
-
Tripartite motif-containing 67, partial [synthetic construct]
Tripartite motif-containing 67, partial [synthetic construct]gi|162318970|gb|AAI56317.1|Protein
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Last Updated: Sep 29, 2024