SERHL2 serine hydrolase like 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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48 |
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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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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 |
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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 | dJ222E13.1 |
MIM | 619045 OMIM |
HGNC | HGNC:29446 HGNC |
Ensembl | ENSG00000183569 Ensembl |
AllianceGenome | HGNC:29446 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000335879.5 | hg38 | chr22 | 42,554,021 | 42,574,055 | 20,035 |
ENST00000327678.10 | hg38 | chr22 | 42,553,956 | 42,574,382 | 20,427 |
ENST00000340239.8 | hg38 | chr22 | 42,553,862 | 42,574,381 | 20,520 |
ENST00000407614.8 | hg38 | chr22 | 42,554,015 | 42,574,165 | 20,151 |
ENST00000340239.8 | hg19 | chr22 | 42,949,868 | 42,970,387 | 20,520 |
ENST00000327678.10 | hg19 | chr22 | 42,949,962 | 42,970,388 | 20,427 |
ENST00000407614.8 | hg19 | chr22 | 42,950,021 | 42,970,171 | 20,151 |
ENST00000335879.5 | hg19 | chr22 | 42,950,027 | 42,970,061 | 20,035 |
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