SUPT20H SPT20 homolog, SAGA complex component
Information
- Symbol
- SUPT20H
- Type
- protein-coding
- Description
- SPT20 homolog, SAGA complex component
- Entrez Gene ID
- 55578
- Genome
- hg19
- Position
- chr13:37,583,630-37,633,786
- Genome
- hg38
- Position
- chr13:37,009,493-37,059,649
- MIM
- 613417 OMIM
- HGNC
- HGNC:20596 HGNC
- Ensembl
- ENSG00000102710 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
risk factor | 0 | 2 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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60 |
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2 |
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 | C13 |
SYNONYM | C13orf19 |
SYNONYM | FAM48A |
SYNONYM | FP757 |
SYNONYM | P38IP |
SYNONYM | SPT20 |
MIM | 613417 OMIM |
HGNC | HGNC:20596 HGNC |
Ensembl | ENSG00000102710 Ensembl |
AllianceGenome | HGNC:20596 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000475892.5 | hg38 | chr13 | 37,009,493 | 37,059,649 | 50,157 |
ENST00000356185.7 | hg38 | chr13 | 37,009,494 | 37,059,650 | 50,157 |
ENST00000350612.11 | hg38 | chr13 | 37,009,312 | 37,059,688 | 50,377 |
ENST00000464744.5 | hg38 | chr13 | 37,009,617 | 37,059,432 | 49,816 |
ENST00000360252.8 | hg38 | chr13 | 37,009,316 | 37,059,713 | 50,398 |
ENST00000350612.11 | hg19 | chr13 | 37,583,449 | 37,633,825 | 50,377 |
ENST00000360252.8 | hg19 | chr13 | 37,583,453 | 37,633,850 | 50,398 |
ENST00000475892.5 | hg19 | chr13 | 37,583,630 | 37,633,786 | 50,157 |
ENST00000356185.7 | hg19 | chr13 | 37,583,631 | 37,633,787 | 50,157 |
ENST00000464744.5 | hg19 | chr13 | 37,583,754 | 37,633,569 | 49,816 |
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