ZNF641 zinc finger protein 641
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 40 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
44 |
 |
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
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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 |
|---|---|
| MIM | 613906 OMIM |
| HGNC | HGNC:31834 HGNC |
| Ensembl | ENSG00000167528 Ensembl |
| AllianceGenome | HGNC:31834 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000448928.7 | hg38 | chr12 | 48,342,421 | 48,351,238 | 8,818 |
| ENST00000547026.6 | hg38 | chr12 | 48,337,180 | 48,350,919 | 13,740 |
| ENST00000544117.6 | hg38 | chr12 | 48,337,180 | 48,350,771 | 13,592 |
| ENST00000301042.7 | hg38 | chr12 | 48,340,008 | 48,350,891 | 10,884 |
| ENST00000544117.6 | hg19 | chr12 | 48,730,963 | 48,744,554 | 13,592 |
| ENST00000547026.6 | hg19 | chr12 | 48,730,963 | 48,744,702 | 13,740 |
| ENST00000301042.7 | hg19 | chr12 | 48,733,791 | 48,744,674 | 10,884 |
| ENST00000448928.7 | hg19 | chr12 | 48,736,204 | 48,745,021 | 8,818 |
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