WDR91 WD repeat domain 91
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 4 |
| Likely pathogenic | 0 | 4 |
| Benign | 0 | 8 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 76 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
94 |
 |
2 |
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
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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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| 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 | HSPC049 |
| SYNONYM | SORF-1 |
| SYNONYM | SORF1 |
| MIM | 616303 OMIM |
| HGNC | HGNC:24997 HGNC |
| Ensembl | ENSG00000105875 Ensembl |
| AllianceGenome | HGNC:24997 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000423565.5 | hg38 | chr7 | 135,183,839 | 135,210,899 | 27,061 |
| ENST00000354475.5 | hg38 | chr7 | 135,183,839 | 135,211,526 | 27,688 |
| ENST00000683848.1 | hg38 | chr7 | 135,183,852 | 135,211,381 | 27,530 |
| ENST00000682802.1 | hg38 | chr7 | 135,183,852 | 135,211,313 | 27,462 |
| ENST00000354475.5 | hg19 | chr7 | 134,868,591 | 134,896,278 | 27,688 |
| ENST00000423565.5 | hg19 | chr7 | 134,868,591 | 134,895,651 | 27,061 |
| ENST00000682802.1 | hg19 | chr7 | 134,868,604 | 134,896,065 | 27,462 |
| ENST00000683848.1 | hg19 | chr7 | 134,868,604 | 134,896,133 | 27,530 |
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