CHTOP chromatin target of PRMT1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 24 |
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
[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 |
Search Word
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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Search word | : | |
Filtering | : |
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 |
---|---|
SYNONYM | C10orf77 |
SYNONYM | C1orf77 |
SYNONYM | FL-SRAG |
SYNONYM | FOP |
SYNONYM | SRAG |
SYNONYM | SRAG-3 |
SYNONYM | SRAG-5 |
SYNONYM | pp7704 |
MIM | 614206 OMIM |
HGNC | HGNC:24511 HGNC |
Ensembl | ENSG00000160679 Ensembl |
AllianceGenome | HGNC:24511 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000368686.1 | hg38 | chr1 | 153,638,342 | 153,644,385 | 6,044 |
ENST00000368687.1 | hg38 | chr1 | 153,638,084 | 153,645,470 | 7,387 |
ENST00000368694.8 | hg38 | chr1 | 153,634,066 | 153,646,306 | 12,241 |
ENST00000368690.7 | hg38 | chr1 | 153,633,982 | 153,646,305 | 12,324 |
ENST00000403433.5 | hg38 | chr1 | 153,634,080 | 153,646,302 | 12,223 |
ENST00000710369.1 | hg38 | chr1 | 153,634,066 | 153,646,306 | 12,241 |
ENST00000614256.4 | hg38 | chr1 | 153,633,982 | 153,646,305 | 12,324 |
ENST00000368690.7 | hg19 | chr1 | 153,606,458 | 153,618,781 | 12,324 |
ENST00000614256.4 | hg19 | chr1 | 153,606,458 | 153,618,781 | 12,324 |
ENST00000368694.8 | hg19 | chr1 | 153,606,542 | 153,618,782 | 12,241 |
ENST00000710369.1 | hg19 | chr1 | 153,606,542 | 153,618,782 | 12,241 |
ENST00000403433.5 | hg19 | chr1 | 153,606,556 | 153,618,778 | 12,223 |
ENST00000368687.1 | hg19 | chr1 | 153,610,560 | 153,617,946 | 7,387 |
ENST00000368686.1 | hg19 | chr1 | 153,610,818 | 153,616,861 | 6,044 |
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