STIP1 stress induced phosphoprotein 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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44 |
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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 | HEL-S-94n |
SYNONYM | HOP |
SYNONYM | IEF-SSP-3521 |
SYNONYM | P60 |
SYNONYM | STI1 |
SYNONYM | STI1L |
MIM | 605063 OMIM |
HGNC | HGNC:11387 HGNC |
Ensembl | ENSG00000168439 Ensembl |
AllianceGenome | HGNC:11387 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000358794.9 | hg38 | chr11 | 64,185,272 | 64,204,543 | 19,272 |
ENST00000543847.1 | hg38 | chr11 | 64,186,225 | 64,195,876 | 9,652 |
ENST00000538945.5 | hg38 | chr11 | 64,186,204 | 64,204,408 | 18,205 |
ENST00000305218.9 | hg38 | chr11 | 64,186,171 | 64,204,543 | 18,373 |
ENST00000358794.9 | hg19 | chr11 | 63,952,744 | 63,972,015 | 19,272 |
ENST00000305218.9 | hg19 | chr11 | 63,953,643 | 63,972,015 | 18,373 |
ENST00000538945.5 | hg19 | chr11 | 63,953,676 | 63,971,880 | 18,205 |
ENST00000543847.1 | hg19 | chr11 | 63,953,697 | 63,963,348 | 9,652 |
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