ACTB actin beta
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 4 | 100 |
| Likely pathogenic | 0 | 152 |
| Benign | 6 | 102 |
| Likely benign | 0 | 478 |
| Conflicting classifications of pathogenicity | 0 | 38 |
| not provided | 0 | 2 |
| Uncertain significance | 0 | 232 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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176 |
![]() |
786 |
![]() |
54 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| 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
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| 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
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| Category | : |
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| 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 | BKRNS |
| SYNONYM | BNS |
| SYNONYM | BRWS1 |
| SYNONYM | CSMH |
| SYNONYM | DDS1 |
| SYNONYM | PS1TP5BP1 |
| SYNONYM | THC8 |
| MIM | 102630 OMIM |
| HGNC | HGNC:132 HGNC |
| Ensembl | ENSG00000075624 Ensembl |
| AllianceGenome | HGNC:132 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000493945.6 | hg38 | chr7 | 5,527,536 | 5,530,602 | 3,067 |
| ENST00000646664.1 | hg38 | chr7 | 5,527,148 | 5,530,601 | 3,454 |
| ENST00000473257.3 | hg38 | chr7 | 5,527,147 | 5,530,604 | 3,458 |
| ENST00000642480.2 | hg38 | chr7 | 5,527,147 | 5,529,949 | 2,803 |
| ENST00000676319.1 | hg38 | chr7 | 5,527,147 | 5,530,604 | 3,458 |
| ENST00000676397.1 | hg38 | chr7 | 5,527,147 | 5,530,581 | 3,435 |
| ENST00000674681.1 | hg38 | chr7 | 5,526,409 | 5,530,601 | 4,193 |
| ENST00000675515.1 | hg38 | chr7 | 5,527,152 | 5,563,902 | 36,751 |
| ENST00000432588.6 | hg38 | chr7 | 5,527,798 | 5,530,627 | 2,830 |
| ENST00000642480.2 | hg19 | chr7 | 5,566,778 | 5,569,580 | 2,803 |
| ENST00000432588.6 | hg19 | chr7 | 5,567,429 | 5,570,258 | 2,830 |
| ENST00000473257.3 | hg19 | chr7 | 5,566,778 | 5,570,235 | 3,458 |
| ENST00000493945.6 | hg19 | chr7 | 5,567,167 | 5,570,233 | 3,067 |
| ENST00000646664.1 | hg19 | chr7 | 5,566,779 | 5,570,232 | 3,454 |
| ENST00000675515.1 | hg19 | chr7 | 5,566,783 | 5,603,533 | 36,751 |
| ENST00000674681.1 | hg19 | chr7 | 5,566,040 | 5,570,232 | 4,193 |
| ENST00000676319.1 | hg19 | chr7 | 5,566,778 | 5,570,235 | 3,458 |
| ENST00000676397.1 | hg19 | chr7 | 5,566,778 | 5,570,212 | 3,435 |
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