API5 apoptosis inhibitor 5
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
16 |
![]() |
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 | AAC-11 |
SYNONYM | AAC11 |
MIM | 609774 OMIM |
HGNC | HGNC:594 HGNC |
Ensembl | ENSG00000166181 Ensembl |
AllianceGenome | HGNC:594 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000534600.5 | hg38 | chr11 | 43,312,096 | 43,336,230 | 24,135 |
ENST00000420461.6 | hg38 | chr11 | 43,311,998 | 43,342,981 | 30,984 |
ENST00000534695.5 | hg38 | chr11 | 43,311,963 | 43,342,676 | 30,714 |
ENST00000531273.6 | hg38 | chr11 | 43,311,996 | 43,344,529 | 32,534 |
ENST00000378852.7 | hg38 | chr11 | 43,312,003 | 43,344,529 | 32,527 |
ENST00000455725.6 | hg38 | chr11 | 43,311,978 | 43,342,980 | 31,003 |
ENST00000534695.5 | hg19 | chr11 | 43,333,513 | 43,364,226 | 30,714 |
ENST00000455725.6 | hg19 | chr11 | 43,333,528 | 43,364,530 | 31,003 |
ENST00000531273.6 | hg19 | chr11 | 43,333,546 | 43,366,079 | 32,534 |
ENST00000420461.6 | hg19 | chr11 | 43,333,548 | 43,364,531 | 30,984 |
ENST00000378852.7 | hg19 | chr11 | 43,333,553 | 43,366,079 | 32,527 |
ENST00000534600.5 | hg19 | chr11 | 43,333,646 | 43,357,780 | 24,135 |
Genome browser