RASGRP3 RAS guanyl releasing protein 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 8 |
association | 0 | 2 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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72 |
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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 | GRP3 |
MIM | 609531 OMIM |
HGNC | HGNC:14545 HGNC |
Ensembl | ENSG00000152689 Ensembl |
AllianceGenome | HGNC:14545 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000407811.5 | hg38 | chr2 | 33,513,875 | 33,564,605 | 50,731 |
ENST00000402538.7 | hg38 | chr2 | 33,436,324 | 33,564,750 | 128,427 |
ENST00000403687.8 | hg38 | chr2 | 33,476,649 | 33,564,731 | 88,083 |
ENST00000402538.7 | hg19 | chr2 | 33,661,391 | 33,789,817 | 128,427 |
ENST00000403687.8 | hg19 | chr2 | 33,701,716 | 33,789,798 | 88,083 |
ENST00000407811.5 | hg19 | chr2 | 33,738,942 | 33,789,672 | 50,731 |
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