ZNF235 zinc finger protein 235
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 14 |
not provided | 1 | 2 |
Uncertain significance | 0 | 150 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
166 |
![]() |
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 |
Type | ID |
---|---|
SYNONYM | ANF270 |
SYNONYM | HZF6 |
SYNONYM | ZFP93 |
SYNONYM | ZNF270 |
MIM | 604749 OMIM |
HGNC | HGNC:12866 HGNC |
Ensembl | ENSG00000159917 Ensembl |
AllianceGenome | HGNC:12866 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000650576.1 | hg38 | chr19 | 44,286,364 | 44,305,025 | 18,662 |
ENST00000589248.5 | hg38 | chr19 | 44,274,752 | 44,305,046 | 30,295 |
ENST00000291182.9 | hg38 | chr19 | 44,286,348 | 44,305,025 | 18,678 |
ENST00000589799.5 | hg38 | chr19 | 44,236,110 | 44,305,019 | 68,910 |
ENST00000589799.5 | hg19 | chr19 | 44,740,263 | 44,809,172 | 68,910 |
ENST00000589248.5 | hg19 | chr19 | 44,778,905 | 44,809,199 | 30,295 |
ENST00000291182.9 | hg19 | chr19 | 44,790,501 | 44,809,178 | 18,678 |
ENST00000650576.1 | hg19 | chr19 | 44,790,517 | 44,809,178 | 18,662 |
Genome browser