PRMT8 protein arginine methyltransferase 8
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
not provided | 1 | 0 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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26 |
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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
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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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 | HRMT1L3 |
SYNONYM | HRMT1L4 |
MIM | 610086 OMIM |
HGNC | HGNC:5188 HGNC |
Ensembl | ENSG00000111218 Ensembl |
AllianceGenome | HGNC:5188 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000382622.4 | hg38 | chr12 | 3,491,203 | 3,593,973 | 102,771 |
ENST00000452611.6 | hg38 | chr12 | 3,381,349 | 3,593,182 | 211,834 |
ENST00000452611.6 | hg19 | chr12 | 3,490,515 | 3,702,348 | 211,834 |
ENST00000382622.4 | hg19 | chr12 | 3,600,369 | 3,703,139 | 102,771 |
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