MRGPRF MAS related GPR family member F
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 50 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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56 |
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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 |
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 | GPR140 |
SYNONYM | GPR168 |
SYNONYM | MRGF |
SYNONYM | RTA |
MIM | 607233 OMIM |
HGNC | HGNC:24828 HGNC |
Ensembl | ENSG00000172935 Ensembl |
AllianceGenome | HGNC:24828 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000309099.7 | hg38 | chr11 | 69,004,398 | 69,013,246 | 8,849 |
ENST00000320913.6 | hg38 | chr11 | 69,009,417 | 69,013,246 | 3,830 |
ENST00000309099.7 | hg19 | chr11 | 68,771,866 | 68,780,714 | 8,849 |
ENST00000320913.6 | hg19 | chr11 | 68,776,885 | 68,780,714 | 3,830 |
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