ZNF322 zinc finger protein 322
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 5 | 0 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | HCG12 |
SYNONYM | ZNF322A |
SYNONYM | ZNF388 |
SYNONYM | ZNF489 |
MIM | 610847 OMIM |
HGNC | HGNC:23640 HGNC |
Ensembl | ENSG00000181315 Ensembl |
AllianceGenome | HGNC:23640 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000471278.5 | hg38 | chr6 | 26,636,291 | 26,651,496 | 15,206 |
ENST00000607204.5 | hg38 | chr6 | 26,634,393 | 26,659,752 | 25,360 |
ENST00000622479.4 | hg38 | chr6 | 26,634,393 | 26,659,752 | 25,360 |
ENST00000456172.5 | hg38 | chr6 | 26,634,393 | 26,659,752 | 25,360 |
ENST00000415922.7 | hg38 | chr6 | 26,634,383 | 26,659,746 | 25,364 |
ENST00000415922.7 | hg19 | chr6 | 26,634,611 | 26,659,974 | 25,364 |
ENST00000456172.5 | hg19 | chr6 | 26,634,621 | 26,659,980 | 25,360 |
ENST00000607204.5 | hg19 | chr6 | 26,634,621 | 26,659,980 | 25,360 |
ENST00000622479.4 | hg19 | chr6 | 26,634,621 | 26,659,980 | 25,360 |
ENST00000471278.5 | hg19 | chr6 | 26,636,519 | 26,651,724 | 15,206 |
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