NM_004750.5(CRLF1):c.966G>A (p.Lys322=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003423457.8
Allele description [Variation Report for NM_004750.5(CRLF1):c.966G>A (p.Lys322=)]
NM_004750.5(CRLF1):c.966G>A (p.Lys322=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens DIS3 like exosome 3'-5' exoribonuclease (DIS3L), transcript variant...
Homo sapiens DIS3 like exosome 3'-5' exoribonuclease (DIS3L), transcript variant 7, mRNAgi|1675115719|ref|NM_001323940.2|Nucleotide
-
SRX24106119 (1)
SRA
-
SRX14011323 (1)
SRA
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Last Updated: Aug 4, 2024