ARHGAP27 Rho GTPase activating protein 27
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 12 |
Uncertain significance | 0 | 90 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
102 |
![]() |
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 | CAMGAP1 |
SYNONYM | PP905 |
SYNONYM | SH3D20 |
SYNONYM | SH3P20 |
MIM | 610591 OMIM |
HGNC | HGNC:31813 HGNC |
Ensembl | ENSG00000159314 Ensembl |
AllianceGenome | HGNC:31813 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000528273.5 | hg38 | chr17 | 45,429,352 | 45,434,421 | 5,070 |
ENST00000376922.6 | hg38 | chr17 | 45,393,909 | 45,425,631 | 31,723 |
ENST00000528677.2 | hg38 | chr17 | 45,393,909 | 45,410,426 | 16,518 |
ENST00000290470.3 | hg38 | chr17 | 45,429,353 | 45,432,916 | 3,564 |
ENST00000685559.1 | hg38 | chr17 | 45,393,908 | 45,432,870 | 38,963 |
ENST00000691061.1 | hg38 | chr17 | 45,393,939 | 45,410,354 | 16,416 |
ENST00000528384.5 | hg38 | chr17 | 45,394,943 | 45,405,934 | 10,992 |
ENST00000532038.5 | hg38 | chr17 | 45,393,902 | 45,410,424 | 16,523 |
ENST00000532891.6 | hg38 | chr17 | 45,395,456 | 45,430,279 | 34,824 |
ENST00000528677.2 | hg19 | chr17 | 43,471,275 | 43,487,792 | 16,518 |
ENST00000532891.6 | hg19 | chr17 | 43,472,822 | 43,507,645 | 34,824 |
ENST00000290470.3 | hg19 | chr17 | 43,506,719 | 43,510,282 | 3,564 |
ENST00000376922.6 | hg19 | chr17 | 43,471,275 | 43,502,997 | 31,723 |
ENST00000528273.5 | hg19 | chr17 | 43,506,718 | 43,511,787 | 5,070 |
ENST00000528384.5 | hg19 | chr17 | 43,472,309 | 43,483,300 | 10,992 |
ENST00000532038.5 | hg19 | chr17 | 43,471,268 | 43,487,790 | 16,523 |
ENST00000691061.1 | hg19 | chr17 | 43,471,305 | 43,487,720 | 16,416 |
ENST00000685559.1 | hg19 | chr17 | 43,471,274 | 43,510,236 | 38,963 |
Genome browser