MAP1S microtubule associated protein 1S
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 14 |
Uncertain significance | 0 | 152 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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168 |
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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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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 | BPY2IP1 |
SYNONYM | C19orf5 |
SYNONYM | MAP8 |
SYNONYM | VCY2IP-1 |
SYNONYM | VCY2IP1 |
MIM | 607573 OMIM |
HGNC | HGNC:15715 HGNC |
Ensembl | ENSG00000130479 Ensembl |
AllianceGenome | HGNC:15715 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000544059.2 | hg38 | chr19 | 17,720,156 | 17,734,490 | 14,335 |
ENST00000324096.9 | hg38 | chr19 | 17,719,480 | 17,734,513 | 15,034 |
ENST00000324096.9 | hg19 | chr19 | 17,830,289 | 17,845,322 | 15,034 |
ENST00000544059.2 | hg19 | chr19 | 17,830,965 | 17,845,299 | 14,335 |
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