ZIC3 Zic family member 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 52 |
Likely pathogenic | 0 | 14 |
Benign | 0 | 34 |
Likely benign | 0 | 56 |
Conflicting classifications of pathogenicity | 0 | 18 |
not provided | 6 | 0 |
Uncertain significance | 0 | 112 |
Ranking
ClinVar | |
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0 |
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0 |
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30 |
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194 |
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22 |
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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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 | HTX |
SYNONYM | HTX1 |
SYNONYM | VACTERLX |
SYNONYM | ZNF203 |
MIM | 300265 OMIM |
HGNC | HGNC:12874 HGNC |
Ensembl | ENSG00000156925 Ensembl |
AllianceGenome | HGNC:12874 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000370606.3 | hg38 | chrX | 137,566,518 | 137,577,691 | 11,174 |
ENST00000287538.10 | hg38 | chrX | 137,566,127 | 137,572,102 | 5,976 |
ENST00000287538.10 | hg19 | chrX | 136,648,286 | 136,654,261 | 5,976 |
ENST00000370606.3 | hg19 | chrX | 136,648,677 | 136,659,850 | 11,174 |
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