ZNF496-DT ZNF496 divergent transcript
Information
- Symbol
- ZNF496-DT
- Type
- ncRNA
- Description
- ZNF496 divergent transcript
- Entrez Gene ID
- 107985115
- Genome
- hg19
- Position
- chr1:247,495,877-247,540,518
- Genome
- hg38
- Position
- chr1:247,332,575-247,377,216
- HGNC
- HGNC:55991 HGNC
- Ensembl
- ENSG00000289234 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
---|
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
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 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000697403.1 | hg38 | chr1 | 247,353,953 | 247,360,818 | 6,866 |
ENST00000697406.1 | hg38 | chr1 | 247,365,177 | 247,393,596 | 28,420 |
ENST00000697395.1 | hg38 | chr1 | 247,332,398 | 247,393,789 | 61,392 |
ENST00000697393.1 | hg38 | chr1 | 247,332,351 | 247,377,221 | 44,871 |
ENST00000697397.1 | hg38 | chr1 | 247,332,765 | 247,393,535 | 60,771 |
ENST00000697396.1 | hg38 | chr1 | 247,332,575 | 247,377,216 | 44,642 |
ENST00000697393.1 | hg19 | chr1 | 247,495,653 | 247,540,523 | 44,871 |
ENST00000697395.1 | hg19 | chr1 | 247,495,700 | 247,557,091 | 61,392 |
ENST00000697396.1 | hg19 | chr1 | 247,495,877 | 247,540,518 | 44,642 |
ENST00000697397.1 | hg19 | chr1 | 247,496,067 | 247,556,837 | 60,771 |
ENST00000697403.1 | hg19 | chr1 | 247,517,255 | 247,524,120 | 6,866 |
ENST00000697406.1 | hg19 | chr1 | 247,528,479 | 247,556,898 | 28,420 |
Genome browser