DCTN6 dynactin subunit 6
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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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 | |||
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Entry | Origin | Type | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | WS-3 |
SYNONYM | WS3 |
SYNONYM | p27 |
MIM | 612963 OMIM |
HGNC | HGNC:16964 HGNC |
Ensembl | ENSG00000104671 Ensembl |
AllianceGenome | HGNC:16964 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000520829.5 | hg38 | chr8 | 30,156,369 | 30,181,021 | 24,653 |
ENST00000221114.8 | hg38 | chr8 | 30,156,369 | 30,183,639 | 27,271 |
ENST00000520829.5 | hg19 | chr8 | 30,013,885 | 30,038,537 | 24,653 |
ENST00000221114.8 | hg19 | chr8 | 30,013,885 | 30,041,155 | 27,271 |
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