ATP8B1-AS1 ATP8B1 antisense RNA 1
Information
- Symbol
- ATP8B1-AS1
- Type
- ncRNA
- Description
- ATP8B1 antisense RNA 1
- Entrez Gene ID
- 100505549
- Genome
- hg19
- Position
- chr18:55,297,582-55,336,528
- Genome
- hg38
- Position
- chr18:57,630,350-57,669,296
- HGNC
- HGNC:56042 HGNC
- Ensembl
- ENSG00000267040 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 3 | 0 |
Likely pathogenic | 1 | 0 |
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
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 |
---|---|---|---|---|---|
ENST00000592201.1 | hg38 | chr18 | 57,630,350 | 57,669,296 | 38,947 |
ENST00000591854.5 | hg38 | chr18 | 57,630,302 | 57,667,636 | 37,335 |
ENST00000591854.5 | hg19 | chr18 | 55,297,534 | 55,334,868 | 37,335 |
ENST00000592201.1 | hg19 | chr18 | 55,297,582 | 55,336,528 | 38,947 |
Genome browser