chr13:32889223:> Detail (hg19) (BRCA2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr13:32,889,223-32,974,405 |
hg38 | chr13:32,315,086-32,400,268 |
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 |
---|---|---|---|---|---|---|---|---|---|
glioblastoma | Temozolomide,Olaparib | C |
![]() |
![]() |
Sensitivity/Response |
![]() |
3 | 31619547 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
In a case report, a 3‐year‐old girl with glioblastoma harboring a probable germline heterozygous BRC... | 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
- hg19
- Position
- chr13:32,889,223-32,974,405
- Variant Type
- snv
- Variant (CIViC) (CIViC Variant)
- COPY-NEUTRAL LOSS OF HETEROZYGOSITY
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/2379
- Variant (CIViC) (CIViC Variant)
- K3226*
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/2871
Genome browser