PRMT1 protein arginine methyltransferase 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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 | ANM1 |
SYNONYM | HCP1 |
SYNONYM | HRMT1L2 |
SYNONYM | IR1B4 |
MIM | 602950 OMIM |
HGNC | HGNC:5187 HGNC |
Ensembl | ENSG00000126457 Ensembl |
AllianceGenome | HGNC:5187 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000454376.7 | hg38 | chr19 | 49,677,271 | 49,688,447 | 11,177 |
ENST00000610806.4 | hg38 | chr19 | 49,677,152 | 49,688,450 | 11,299 |
ENST00000532489.5 | hg38 | chr19 | 49,675,897 | 49,688,447 | 12,551 |
ENST00000391851.8 | hg38 | chr19 | 49,677,152 | 49,688,447 | 11,296 |
ENST00000391851.8 | hg19 | chr19 | 50,180,409 | 50,191,704 | 11,296 |
ENST00000454376.7 | hg19 | chr19 | 50,180,528 | 50,191,704 | 11,177 |
ENST00000532489.5 | hg19 | chr19 | 50,179,154 | 50,191,704 | 12,551 |
ENST00000610806.4 | hg19 | chr19 | 50,180,409 | 50,191,707 | 11,299 |
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