DAP3 death associated protein 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Likely pathogenic | 0 | 4 |
Benign | 0 | 14 |
Likely benign | 0 | 26 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
6 |
![]() |
100 |
![]() |
2 |
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 | DAP-3 |
SYNONYM | MRP-S29 |
SYNONYM | MRPS29 |
SYNONYM | S29mt |
SYNONYM | bMRP-10 |
SYNONYM | mS29 |
MIM | 602074 OMIM |
HGNC | HGNC:2673 HGNC |
Ensembl | ENSG00000132676 Ensembl |
AllianceGenome | HGNC:2673 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000465375.5 | hg38 | chr1 | 155,689,094 | 155,721,989 | 32,896 |
ENST00000343043.7 | hg38 | chr1 | 155,689,083 | 155,738,526 | 49,444 |
ENST00000368336.10 | hg38 | chr1 | 155,689,091 | 155,739,010 | 49,920 |
ENST00000535183.5 | hg38 | chr1 | 155,689,091 | 155,738,971 | 49,881 |
ENST00000421487.6 | hg38 | chr1 | 155,689,091 | 155,738,526 | 49,436 |
ENST00000471642.6 | hg38 | chr1 | 155,687,967 | 155,738,526 | 50,560 |
ENST00000471642.6 | hg19 | chr1 | 155,657,758 | 155,708,317 | 50,560 |
ENST00000343043.7 | hg19 | chr1 | 155,658,874 | 155,708,317 | 49,444 |
ENST00000368336.10 | hg19 | chr1 | 155,658,882 | 155,708,801 | 49,920 |
ENST00000421487.6 | hg19 | chr1 | 155,658,882 | 155,708,317 | 49,436 |
ENST00000465375.5 | hg19 | chr1 | 155,658,885 | 155,691,780 | 32,896 |
ENST00000535183.5 | hg19 | chr1 | 155,658,882 | 155,708,762 | 49,881 |
Genome browser