NM_001457.4(FLNB):c.2055+221G>A AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 26, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001616603.3
Allele description [Variation Report for NM_001457.4(FLNB):c.2055+221G>A]
NM_001457.4(FLNB):c.2055+221G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Acronychia anomala (5)
Nucleotide
-
nssv2845432 (2)
dbVar
-
C2orf69 chromosome 2 open reading frame 69 [Homo sapiens]
C2orf69 chromosome 2 open reading frame 69 [Homo sapiens]Gene ID:205327Gene
-
Gene Links for GEO Profiles (Select 126387671) (1)
Gene
-
Mutant HLA-F-adjacent transcript 10 overexpression effect on HCT116 colon cancer...
Mutant HLA-F-adjacent transcript 10 overexpression effect on HCT116 colon cancer cell lineAccession: GDS5439GEO DataSets
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023