ZNF254 zinc finger protein 254
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 122 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
124 |
![]() |
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 | BMZF-5 |
SYNONYM | HD-ZNF1 |
SYNONYM | ZNF539 |
SYNONYM | ZNF91L |
MIM | 604768 OMIM |
HGNC | HGNC:13047 HGNC |
Ensembl | ENSG00000213096 Ensembl |
AllianceGenome | HGNC:13047 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000357002.5 | hg38 | chr19 | 24,087,187 | 24,129,968 | 42,782 |
ENST00000613065.4 | hg38 | chr19 | 24,033,405 | 24,129,961 | 96,557 |
ENST00000339642.10 | hg38 | chr19 | 24,087,184 | 24,107,349 | 20,166 |
ENST00000616028.2 | hg38 | chr19 | 24,087,160 | 24,129,961 | 42,802 |
ENST00000611359.3 | hg38 | chr19 | 24,087,160 | 24,129,961 | 42,802 |
ENST00000613065.4 | hg19 | chr19 | 24,216,207 | 24,312,763 | 96,557 |
ENST00000611359.3 | hg19 | chr19 | 24,269,962 | 24,312,763 | 42,802 |
ENST00000616028.2 | hg19 | chr19 | 24,269,962 | 24,312,763 | 42,802 |
ENST00000339642.10 | hg19 | chr19 | 24,269,986 | 24,290,151 | 20,166 |
ENST00000357002.5 | hg19 | chr19 | 24,269,989 | 24,312,770 | 42,782 |
Genome browser