MAGT1 magnesium transporter 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 46 |
Likely pathogenic | 0 | 16 |
Benign | 0 | 56 |
Likely benign | 0 | 120 |
Conflicting classifications of pathogenicity | 0 | 16 |
not provided | 6 | 0 |
Uncertain significance | 0 | 178 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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40 |
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348 |
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20 |
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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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 | CDG1CC |
SYNONYM | IAP |
SYNONYM | MRX95 |
SYNONYM | OST3B |
SYNONYM | PRO0756 |
SYNONYM | SLC58A1 |
SYNONYM | XMEN |
SYNONYM | bA217H1.1 |
MIM | 300715 OMIM |
HGNC | HGNC:28880 HGNC |
Ensembl | ENSG00000102158 Ensembl |
AllianceGenome | HGNC:28880 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000618282.5 | hg38 | chrX | 77,825,747 | 77,895,435 | 69,689 |
ENST00000685353.1 | hg38 | chrX | 77,827,594 | 77,895,437 | 67,844 |
ENST00000358075.11 | hg38 | chrX | 77,826,364 | 77,895,593 | 69,230 |
ENST00000685015.1 | hg38 | chrX | 77,826,409 | 77,895,437 | 69,029 |
ENST00000373336.3 | hg38 | chrX | 77,868,108 | 77,895,440 | 27,333 |
ENST00000692161.1 | hg38 | chrX | 77,826,388 | 77,895,448 | 69,061 |
ENST00000688650.1 | hg38 | chrX | 77,826,693 | 77,895,437 | 68,745 |
ENST00000689519.1 | hg38 | chrX | 77,827,435 | 77,895,437 | 68,003 |
ENST00000618282.5 | hg19 | chrX | 77,081,244 | 77,150,932 | 69,689 |
ENST00000358075.11 | hg19 | chrX | 77,081,861 | 77,151,090 | 69,230 |
ENST00000692161.1 | hg19 | chrX | 77,081,885 | 77,150,945 | 69,061 |
ENST00000685015.1 | hg19 | chrX | 77,081,906 | 77,150,934 | 69,029 |
ENST00000688650.1 | hg19 | chrX | 77,082,190 | 77,150,934 | 68,745 |
ENST00000689519.1 | hg19 | chrX | 77,082,932 | 77,150,934 | 68,003 |
ENST00000685353.1 | hg19 | chrX | 77,083,091 | 77,150,934 | 67,844 |
ENST00000373336.3 | hg19 | chrX | 77,123,605 | 77,150,937 | 27,333 |
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