GRP gastrin releasing peptide
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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10 |
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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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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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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 | BN |
SYNONYM | GRP-10 |
SYNONYM | preproGRP |
SYNONYM | proGRP |
MIM | 137260 OMIM |
HGNC | HGNC:4605 HGNC |
Ensembl | ENSG00000134443 Ensembl |
AllianceGenome | HGNC:4605 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000420468.6 | hg38 | chr18 | 59,220,266 | 59,230,621 | 10,356 |
ENST00000529320.2 | hg38 | chr18 | 59,220,172 | 59,230,770 | 10,599 |
ENST00000256857.7 | hg38 | chr18 | 59,220,158 | 59,230,771 | 10,614 |
ENST00000256857.7 | hg19 | chr18 | 56,887,390 | 56,898,003 | 10,614 |
ENST00000529320.2 | hg19 | chr18 | 56,887,404 | 56,898,002 | 10,599 |
ENST00000420468.6 | hg19 | chr18 | 56,887,498 | 56,897,853 | 10,356 |
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