FSCN1 fascin actin-bundling protein 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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40 |
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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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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | FAN1 |
SYNONYM | HSN |
SYNONYM | SNL |
SYNONYM | p55 |
MIM | 602689 OMIM |
HGNC | HGNC:11148 HGNC |
Ensembl | ENSG00000075618 Ensembl |
AllianceGenome | HGNC:11148 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000382361.8 | hg38 | chr7 | 5,592,816 | 5,606,655 | 13,840 |
ENST00000382361.8 | hg19 | chr7 | 5,632,447 | 5,646,286 | 13,840 |
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