PFDN6 prefoldin subunit 6
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 12 |
| Uncertain significance | 0 | 80 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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98 |
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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 | |||||||||||
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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 | H2-KE2 |
| SYNONYM | HKE2 |
| SYNONYM | KE-2 |
| SYNONYM | PFD6 |
| MIM | 605660 OMIM |
| HGNC | HGNC:4926 HGNC |
| Ensembl | ENSG00000204220 Ensembl |
| AllianceGenome | HGNC:4926 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000374606.10 | hg38 | chr6 | 33,289,601 | 33,290,933 | 1,333 |
| ENST00000374610.6 | hg38 | chr6 | 33,289,597 | 33,290,862 | 1,266 |
| ENST00000395131.5 | hg38 | chr6 | 33,289,302 | 33,290,933 | 1,632 |
| ENST00000463584.1 | hg38 | chr6 | 33,289,775 | 33,298,401 | 8,627 |
| ENST00000374607.5 | hg38 | chr6 | 33,289,597 | 33,290,934 | 1,338 |
| ENST00000395131.5 | hg19 | chr6 | 33,257,079 | 33,258,710 | 1,632 |
| ENST00000374610.6 | hg19 | chr6 | 33,257,374 | 33,258,639 | 1,266 |
| ENST00000374607.5 | hg19 | chr6 | 33,257,374 | 33,258,711 | 1,338 |
| ENST00000374606.10 | hg19 | chr6 | 33,257,378 | 33,258,710 | 1,333 |
| ENST00000463584.1 | hg19 | chr6 | 33,257,552 | 33,266,178 | 8,627 |
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