HSPBP1 HSPA (Hsp70) binding protein 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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60 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | FES1 |
MIM | 612939 OMIM |
HGNC | HGNC:24989 HGNC |
Ensembl | ENSG00000133265 Ensembl |
AllianceGenome | HGNC:24989 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000433386.7 | hg38 | chr19 | 55,262,223 | 55,280,110 | 17,888 |
ENST00000587922.5 | hg38 | chr19 | 55,262,487 | 55,279,856 | 17,370 |
ENST00000255631.9 | hg38 | chr19 | 55,262,231 | 55,280,360 | 18,130 |
ENST00000433386.7 | hg19 | chr19 | 55,773,591 | 55,791,478 | 17,888 |
ENST00000255631.9 | hg19 | chr19 | 55,773,599 | 55,791,728 | 18,130 |
ENST00000587922.5 | hg19 | chr19 | 55,773,855 | 55,791,224 | 17,370 |
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