MT1B metallothionein 1B
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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12 |
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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
[No Data.]
Locus Zoom
Variants
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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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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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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 | MT-1B |
SYNONYM | MT-IB |
SYNONYM | MT1 |
SYNONYM | MT1Q |
SYNONYM | MTP |
MIM | 156349 OMIM |
HGNC | HGNC:7394 HGNC |
Ensembl | ENSG00000169688 Ensembl |
AllianceGenome | HGNC:7394 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000334346.3 | hg38 | chr16 | 56,651,886 | 56,653,204 | 1,319 |
ENST00000562399.1 | hg38 | chr16 | 56,651,926 | 56,653,204 | 1,279 |
ENST00000334346.3 | hg19 | chr16 | 56,685,798 | 56,687,116 | 1,319 |
ENST00000562399.1 | hg19 | chr16 | 56,685,838 | 56,687,116 | 1,279 |
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