GRAP2 GRB2 related adaptor protein 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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42 |
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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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Filtering | : |
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 |
---|---|
SYNONYM | GADS |
SYNONYM | GRAP-2 |
SYNONYM | GRB2L |
SYNONYM | GRBLG |
SYNONYM | GRID |
SYNONYM | GRPL |
SYNONYM | GrbX |
SYNONYM | Grf40 |
SYNONYM | Mona |
SYNONYM | P38 |
MIM | 604518 OMIM |
HGNC | HGNC:4563 HGNC |
Ensembl | ENSG00000100351 Ensembl |
AllianceGenome | HGNC:4563 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000407075.3 | hg38 | chr22 | 39,946,817 | 39,971,105 | 24,289 |
ENST00000344138.9 | hg38 | chr22 | 39,901,084 | 39,973,721 | 72,638 |
ENST00000344138.9 | hg19 | chr22 | 40,297,088 | 40,369,725 | 72,638 |
ENST00000407075.3 | hg19 | chr22 | 40,342,821 | 40,367,109 | 24,289 |
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