SOX15 SRY-box transcription factor 15
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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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 |
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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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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 | SOX20 |
SYNONYM | SOX26 |
SYNONYM | SOX27 |
MIM | 601297 OMIM |
HGNC | HGNC:11196 HGNC |
Ensembl | ENSG00000129194 Ensembl |
AllianceGenome | HGNC:11196 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000570788.1 | hg38 | chr17 | 7,588,999 | 7,590,091 | 1,093 |
ENST00000250055.3 | hg38 | chr17 | 7,588,178 | 7,590,094 | 1,917 |
ENST00000538513.6 | hg38 | chr17 | 7,588,178 | 7,590,072 | 1,895 |
ENST00000538513.6 | hg19 | chr17 | 7,491,496 | 7,493,390 | 1,895 |
ENST00000250055.3 | hg19 | chr17 | 7,491,496 | 7,493,412 | 1,917 |
ENST00000570788.1 | hg19 | chr17 | 7,492,317 | 7,493,409 | 1,093 |
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