ZSCAN10 zinc finger and SCAN domain containing 10
Information
- Symbol
- ZSCAN10
- Type
- protein-coding
- Description
- zinc finger and SCAN domain containing 10
- Entrez Gene ID
- 84891
- Genome
- hg19
- Position
- chr16:3,138,891-3,149,295
- Genome
- hg38
- Position
- chr16:3,088,890-3,099,294
- MIM
- 618365 OMIM
- HGNC
- HGNC:12997 HGNC
- Ensembl
- ENSG00000130182 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Benign | 0 | 12 |
Likely benign | 0 | 20 |
Uncertain significance | 0 | 100 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
4 |
![]() |
128 |
![]() |
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
|
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 | ZFP206 |
SYNONYM | ZNF206 |
MIM | 618365 OMIM |
HGNC | HGNC:12997 HGNC |
Ensembl | ENSG00000130182 Ensembl |
AllianceGenome | HGNC:12997 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000575108.5 | hg38 | chr16 | 3,088,894 | 3,099,292 | 10,399 |
ENST00000576985.6 | hg38 | chr16 | 3,088,890 | 3,099,294 | 10,405 |
ENST00000252463.6 | hg38 | chr16 | 3,088,894 | 3,092,860 | 3,967 |
ENST00000572548.1 | hg38 | chr16 | 3,090,552 | 3,099,261 | 8,710 |
ENST00000538082.5 | hg38 | chr16 | 3,088,989 | 3,099,295 | 10,307 |
ENST00000576985.6 | hg19 | chr16 | 3,138,891 | 3,149,295 | 10,405 |
ENST00000252463.6 | hg19 | chr16 | 3,138,895 | 3,142,861 | 3,967 |
ENST00000575108.5 | hg19 | chr16 | 3,138,895 | 3,149,293 | 10,399 |
ENST00000538082.5 | hg19 | chr16 | 3,138,990 | 3,149,296 | 10,307 |
ENST00000572548.1 | hg19 | chr16 | 3,140,553 | 3,149,262 | 8,710 |
Genome browser