ZNRF3 zinc and ring finger 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 10 |
not provided | 9 | 0 |
Uncertain significance | 0 | 102 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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116 |
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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 |
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Target data | : |
MGeND data only
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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 | BK747E2.3 |
SYNONYM | RNF203 |
MIM | 612062 OMIM |
HGNC | HGNC:18126 HGNC |
Ensembl | ENSG00000183579 Ensembl |
AllianceGenome | HGNC:18126 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000406323.3 | hg38 | chr22 | 28,987,052 | 29,053,965 | 66,914 |
ENST00000402174.5 | hg38 | chr22 | 28,917,389 | 29,053,685 | 136,297 |
ENST00000544604.7 | hg38 | chr22 | 28,883,572 | 29,057,488 | 173,917 |
ENST00000544604.7 | hg19 | chr22 | 29,279,560 | 29,453,476 | 173,917 |
ENST00000402174.5 | hg19 | chr22 | 29,313,377 | 29,449,673 | 136,297 |
ENST00000406323.3 | hg19 | chr22 | 29,383,040 | 29,449,953 | 66,914 |
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