MCRS1 microspherule protein 1
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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24 |
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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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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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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 | ICP22BP |
SYNONYM | INO80Q |
SYNONYM | MCRS2 |
SYNONYM | MSP58 |
SYNONYM | P78 |
MIM | 609504 OMIM |
HGNC | HGNC:6960 HGNC |
Ensembl | ENSG00000187778 Ensembl |
AllianceGenome | HGNC:6960 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000343810.9 | hg38 | chr12 | 49,558,299 | 49,568,142 | 9,844 |
ENST00000546244.5 | hg38 | chr12 | 49,558,295 | 49,568,145 | 9,851 |
ENST00000550165.5 | hg38 | chr12 | 49,558,363 | 49,568,101 | 9,739 |
ENST00000357123.8 | hg38 | chr12 | 49,558,643 | 49,566,439 | 7,797 |
ENST00000546244.5 | hg19 | chr12 | 49,952,078 | 49,961,928 | 9,851 |
ENST00000343810.9 | hg19 | chr12 | 49,952,082 | 49,961,925 | 9,844 |
ENST00000550165.5 | hg19 | chr12 | 49,952,146 | 49,961,884 | 9,739 |
ENST00000357123.8 | hg19 | chr12 | 49,952,426 | 49,960,222 | 7,797 |
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