GRCh38/hg38 Xp22.33(chrX:3501549-3758140)x1 Detail (hg19) (PRKX, PRKX-AS1, SNORA48B, LOC125446265, LOC126863190, LOC126863191, LOC130067893, LOC130067894, LOC130067895, LOC130067896, LOC130067897, LOC130067898)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chrX:3,419,590-3,676,181 |
| hg38 | chrX:3,501,549-3,758,140 View the variant detail on this assembly version. |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
ClinVar
| Clinical Significance |
Uncertain significance
|
| Review star |  |
| Show details | |
Links
| Type | Database | ID | Link |
|---|---|---|---|
| Gene | MIM | ||
| HGNC | |||
| Ensembl | |||
| NCBI | |||
| Gene Cards | |||
| OncoKB |
| Type | Database | ID | Link |
|---|---|---|---|
| Variant | TogoVar | ||
| COSMIC | |||
| MONDO |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
|
Uncertain significance
|
2011-01-05 | no assertion criteria provided |
not provided
|
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| GRCh38/hg38 Xp22.33(chrX:3501549-3758140)x1 AND See cases | ClinVar | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- Genome
- hg19
- Position
- chrX:3,419,590-3,676,181
- Variant Type
- cnv
Genome browser