VASH2 vasohibin 2
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 36 |
Ranking
| ClinVar | |
|---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
40 |
![]() |
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 |
|---|---|
| MIM | 610471 OMIM |
| HGNC | HGNC:25723 HGNC |
| Ensembl | ENSG00000143494 Ensembl |
| AllianceGenome | HGNC:25723 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000517399.3 | hg38 | chr1 | 212,950,541 | 212,991,585 | 41,045 |
| ENST00000366966.6 | hg38 | chr1 | 212,950,520 | 212,988,698 | 38,179 |
| ENST00000366965.6 | hg38 | chr1 | 212,950,635 | 212,990,910 | 40,276 |
| ENST00000366964.7 | hg38 | chr1 | 212,950,618 | 212,969,249 | 18,632 |
| ENST00000366968.8 | hg38 | chr1 | 212,950,594 | 212,991,585 | 40,992 |
| ENST00000366967.6 | hg38 | chr1 | 212,950,667 | 212,988,924 | 38,258 |
| ENST00000366966.6 | hg19 | chr1 | 213,123,862 | 213,162,040 | 38,179 |
| ENST00000517399.3 | hg19 | chr1 | 213,123,883 | 213,164,927 | 41,045 |
| ENST00000366968.8 | hg19 | chr1 | 213,123,936 | 213,164,927 | 40,992 |
| ENST00000366964.7 | hg19 | chr1 | 213,123,960 | 213,142,591 | 18,632 |
| ENST00000366965.6 | hg19 | chr1 | 213,123,977 | 213,164,252 | 40,276 |
| ENST00000366967.6 | hg19 | chr1 | 213,124,009 | 213,162,266 | 38,258 |
Genome browser




