CFL1 cofilin 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
20 |
![]() |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | CFL |
SYNONYM | HEL-S-15 |
SYNONYM | cofilin |
MIM | 601442 OMIM |
HGNC | HGNC:1874 HGNC |
Ensembl | ENSG00000172757 Ensembl |
AllianceGenome | HGNC:1874 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000308162.10 | hg38 | chr11 | 65,854,673 | 65,858,180 | 3,508 |
ENST00000527344.5 | hg38 | chr11 | 65,854,975 | 65,857,033 | 2,059 |
ENST00000525451.6 | hg38 | chr11 | 65,854,675 | 65,859,415 | 4,741 |
ENST00000534769.5 | hg38 | chr11 | 65,855,241 | 65,861,421 | 6,181 |
ENST00000531407.5 | hg38 | chr11 | 65,855,009 | 65,857,868 | 2,860 |
ENST00000524553.5 | hg38 | chr11 | 65,855,054 | 65,856,964 | 1,911 |
ENST00000531413.5 | hg38 | chr11 | 65,855,257 | 65,859,289 | 4,033 |
ENST00000308162.10 | hg19 | chr11 | 65,622,144 | 65,625,651 | 3,508 |
ENST00000525451.6 | hg19 | chr11 | 65,622,146 | 65,626,886 | 4,741 |
ENST00000527344.5 | hg19 | chr11 | 65,622,446 | 65,624,504 | 2,059 |
ENST00000531407.5 | hg19 | chr11 | 65,622,480 | 65,625,339 | 2,860 |
ENST00000524553.5 | hg19 | chr11 | 65,622,525 | 65,624,435 | 1,911 |
ENST00000534769.5 | hg19 | chr11 | 65,622,712 | 65,628,892 | 6,181 |
ENST00000531413.5 | hg19 | chr11 | 65,622,728 | 65,626,760 | 4,033 |
Genome browser