GNG13 G protein subunit gamma 13
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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10 |
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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 |
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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 | G(gamma)13 |
SYNONYM | HG3J |
SYNONYM | h2-35 |
MIM | 607298 OMIM |
HGNC | HGNC:14131 HGNC |
Ensembl | ENSG00000127588 Ensembl |
AllianceGenome | HGNC:14131 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000248150.5 | hg38 | chr16 | 798,041 | 800,734 | 2,694 |
ENST00000248150.5 | hg19 | chr16 | 848,041 | 850,734 | 2,694 |
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