ZMYM3 zinc finger MYM-type containing 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Benign | 0 | 12 |
Likely benign | 0 | 42 |
Conflicting classifications of pathogenicity | 0 | 8 |
not provided | 6 | 0 |
Uncertain significance | 0 | 132 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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14 |
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168 |
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8 |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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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Search word | : | |
Filtering | : |
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 |
---|---|
SYNONYM | DXS6673E |
SYNONYM | MYM |
SYNONYM | XFIM |
SYNONYM | XLID112 |
SYNONYM | ZNF198L2 |
SYNONYM | ZNF261 |
MIM | 300061 OMIM |
HGNC | HGNC:13054 HGNC |
Ensembl | ENSG00000147130 Ensembl |
AllianceGenome | HGNC:13054 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000373988.5 | hg38 | chrX | 71,239,626 | 71,255,060 | 15,435 |
ENST00000373998.5 | hg38 | chrX | 71,239,624 | 71,255,146 | 15,523 |
ENST00000373978.1 | hg38 | chrX | 71,249,209 | 71,254,539 | 5,331 |
ENST00000373981.5 | hg38 | chrX | 71,249,204 | 71,254,575 | 5,372 |
ENST00000373982.5 | hg38 | chrX | 71,249,201 | 71,254,140 | 4,940 |
ENST00000373984.7 | hg38 | chrX | 71,239,626 | 71,254,129 | 14,504 |
ENST00000314425.9 | hg38 | chrX | 71,239,624 | 71,254,140 | 14,517 |
ENST00000314425.9 | hg19 | chrX | 70,459,474 | 70,473,990 | 14,517 |
ENST00000373998.5 | hg19 | chrX | 70,459,474 | 70,474,996 | 15,523 |
ENST00000373984.7 | hg19 | chrX | 70,459,476 | 70,473,979 | 14,504 |
ENST00000373988.5 | hg19 | chrX | 70,459,476 | 70,474,910 | 15,435 |
ENST00000373982.5 | hg19 | chrX | 70,469,051 | 70,473,990 | 4,940 |
ENST00000373981.5 | hg19 | chrX | 70,469,054 | 70,474,425 | 5,372 |
ENST00000373978.1 | hg19 | chrX | 70,469,059 | 70,474,389 | 5,331 |
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