FGG fibrinogen gamma chain
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 8 | 22 |
Likely pathogenic | 0 | 22 |
Benign | 16 | 22 |
Likely benign | 0 | 38 |
Conflicting classifications of pathogenicity | 0 | 18 |
other | 0 | 16 |
Uncertain significance | 0 | 128 |
Ranking
ClinVar | |
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0 |
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0 |
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28 |
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188 |
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28 |
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
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000405164.5 | hg38 | chr4 | 154,604,173 | 154,612,643 | 8,471 |
ENST00000404648.7 | hg38 | chr4 | 154,604,134 | 154,612,849 | 8,716 |
ENST00000336098.8 | hg38 | chr4 | 154,604,171 | 154,612,656 | 8,486 |
ENST00000407946.5 | hg38 | chr4 | 154,604,610 | 154,612,635 | 8,026 |
ENST00000404648.7 | hg19 | chr4 | 155,525,286 | 155,534,001 | 8,716 |
ENST00000336098.8 | hg19 | chr4 | 155,525,323 | 155,533,808 | 8,486 |
ENST00000405164.5 | hg19 | chr4 | 155,525,325 | 155,533,795 | 8,471 |
ENST00000407946.5 | hg19 | chr4 | 155,525,762 | 155,533,787 | 8,026 |
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