CHST8 carbohydrate sulfotransferase 8
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 6 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 56 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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70 |
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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 |
---|---|
SYNONYM | GALNAC4ST1 |
SYNONYM | GalNAc4ST |
SYNONYM | PSS3 |
MIM | 610190 OMIM |
HGNC | HGNC:15993 HGNC |
Ensembl | ENSG00000124302 Ensembl |
AllianceGenome | HGNC:15993 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000438847.7 | hg38 | chr19 | 33,621,971 | 33,773,509 | 151,539 |
ENST00000434302.5 | hg38 | chr19 | 33,621,955 | 33,773,508 | 151,554 |
ENST00000650847.1 | hg38 | chr19 | 33,621,953 | 33,773,506 | 151,554 |
ENST00000262622.4 | hg38 | chr19 | 33,684,528 | 33,773,509 | 88,982 |
ENST00000650847.1 | hg19 | chr19 | 34,112,859 | 34,264,411 | 151,553 |
ENST00000434302.5 | hg19 | chr19 | 34,112,861 | 34,264,413 | 151,553 |
ENST00000438847.7 | hg19 | chr19 | 34,112,877 | 34,264,414 | 151,538 |
ENST00000262622.4 | hg19 | chr19 | 34,175,434 | 34,264,414 | 88,981 |
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