chr2:111125618:> Detail (hg38) (BCL2L11)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr2:111,883,195-111,886,097 |
hg38 | chr2:111,125,618-111,128,520 |
HGVS
Type | Transcript | Protein |
---|---|---|
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease | Drug | EL | ET | ED | CS | VO | TR | Pubmed | Links |
---|---|---|---|---|---|---|---|---|---|
chronic myeloid leukemia | Imatinib | B |
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Resistance | Common Germline | 4 | 22426421 | Detail |
lung non-small cell carcinoma | Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor | B |
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Resistance | Common Germline | 4 | 22426421 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
DNA sequencing was performed in five Ph+ CML samples with sensitivity or resistance to imatinib. A s... | CIViC Evidence | Detail |
The BIM (BCL2L11) deletion polymorphism was identified in an EGFR Mutant NSCLC cell line with resist... | CIViC Evidence | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- Genome
- hg38
- Position
- chr2:111,125,618-111,128,520
- Variant Type
- snv
- Variant (CIViC) (CIViC Variant)
- DELETION POLYMORPHISM
- Transcript 1 (CIViC Variant)
- ENST00000393256.3
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/526
Genome browser