chr9:95099054:> Detail (hg38) (FANCC)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr9:97,861,336-98,079,984 |
| hg38 | chr9:95,099,054-95,317,702 |
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 |
|---|---|---|---|---|---|---|---|---|---|
| pancreatic cancer | Mitomycin,Cisplatin,Chlorambucil,Melphalan,Gemcitabine | D |
Predictive
|
Supports
|
Sensitivity/Response |
Unknown
|
3 | 16243825 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| In the pancreatic cell lines PL11 (FANCC homozygous deletion) and Hs766T (FANCG-mutated), sensitivit... | CIViC Evidence | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- Genome
- hg38
- Position
- chr9:95,099,054-95,317,702
- Variant Type
- snv
- Variant (CIViC) (CIViC Variant)
- LOSS-OF-FUNCTION
- Transcript 1 (CIViC Variant)
- ENST00000289081.3
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/534
Genome browser