SUPT20HL1 SUPT20H like 1
Information
- Symbol
- SUPT20HL1
- Type
- protein-coding
- Description
- SUPT20H like 1
- Entrez Gene ID
- 100130302
- Genome
- hg19
- Position
- chrX:24,378,756-24,385,956
- Genome
- hg38
- Position
- chrX:24,360,639-24,367,839
- HGNC
- HGNC:30773 HGNC
- Ensembl
- ENSG00000223731 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 14 |
| not provided | 6 | 0 |
Ranking
| ClinVar | |
|---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
12 |
![]() |
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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | FAM48B1 |
| SYNONYM | SPT20L |
| HGNC | HGNC:30773 HGNC |
| Ensembl | ENSG00000223731 Ensembl |
| AllianceGenome | HGNC:30773 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000686983.1 | hg38 | chrX | 24,360,639 | 24,367,839 | 7,201 |
| ENST00000436466.2 | hg38 | chrX | 24,362,325 | 24,365,424 | 3,100 |
| ENST00000686983.1 | hg19 | chrX | 24,378,756 | 24,385,956 | 7,201 |
| ENST00000436466.2 | hg19 | chrX | 24,380,442 | 24,383,541 | 3,100 |
Genome browser




