VEGFA vascular endothelial growth factor A
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 14 |
Likely benign | 0 | 34 |
not provided | 9 | 0 |
other | 0 | 2 |
Uncertain significance | 1 | 48 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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4 |
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92 |
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4 |
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 |
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SYNONYM | L-VEGF |
SYNONYM | MVCD1 |
SYNONYM | VEGF |
SYNONYM | VPF |
MIM | 192240 OMIM |
HGNC | HGNC:12680 HGNC |
Ensembl | ENSG00000112715 Ensembl |
AllianceGenome | HGNC:12680 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000417285.7 | hg38 | chr6 | 43,770,707 | 43,784,562 | 13,856 |
ENST00000523125.5 | hg38 | chr6 | 43,771,247 | 43,784,562 | 13,316 |
ENST00000457104.6 | hg38 | chr6 | 43,771,247 | 43,784,562 | 13,316 |
ENST00000413642.8 | hg38 | chr6 | 43,770,707 | 43,784,589 | 13,883 |
ENST00000672860.3 | hg38 | chr6 | 43,770,211 | 43,786,487 | 16,277 |
ENST00000372077.8 | hg38 | chr6 | 43,770,782 | 43,786,487 | 15,706 |
ENST00000518824.5 | hg38 | chr6 | 43,771,247 | 43,784,658 | 13,412 |
ENST00000523873.5 | hg38 | chr6 | 43,771,209 | 43,784,609 | 13,401 |
ENST00000324450.11 | hg38 | chr6 | 43,770,707 | 43,784,562 | 13,856 |
ENST00000482630.7 | hg38 | chr6 | 43,770,707 | 43,784,658 | 13,952 |
ENST00000523950.5 | hg38 | chr6 | 43,771,209 | 43,784,902 | 13,694 |
ENST00000520948.5 | hg38 | chr6 | 43,771,083 | 43,784,949 | 13,867 |
ENST00000425836.9 | hg38 | chr6 | 43,770,211 | 43,786,487 | 16,277 |
ENST00000518689.5 | hg38 | chr6 | 43,771,247 | 43,784,562 | 13,316 |
ENST00000372064.9 | hg38 | chr6 | 43,770,707 | 43,786,487 | 15,781 |
ENST00000372067.8 | hg38 | chr6 | 43,770,213 | 43,786,487 | 16,275 |
ENST00000230480.10 | hg38 | chr6 | 43,771,992 | 43,784,935 | 12,944 |
ENST00000372055.9 | hg38 | chr6 | 43,770,707 | 43,784,609 | 13,903 |
ENST00000425836.9 | hg19 | chr6 | 43,737,948 | 43,754,224 | 16,277 |
ENST00000230480.10 | hg19 | chr6 | 43,739,729 | 43,752,672 | 12,944 |
ENST00000372055.9 | hg19 | chr6 | 43,738,444 | 43,752,346 | 13,903 |
ENST00000372064.9 | hg19 | chr6 | 43,738,444 | 43,754,224 | 15,781 |
ENST00000372077.8 | hg19 | chr6 | 43,738,519 | 43,754,224 | 15,706 |
ENST00000413642.8 | hg19 | chr6 | 43,738,444 | 43,752,326 | 13,883 |
ENST00000417285.7 | hg19 | chr6 | 43,738,444 | 43,752,299 | 13,856 |
ENST00000324450.11 | hg19 | chr6 | 43,738,444 | 43,752,299 | 13,856 |
ENST00000372067.8 | hg19 | chr6 | 43,737,950 | 43,754,224 | 16,275 |
ENST00000482630.7 | hg19 | chr6 | 43,738,444 | 43,752,395 | 13,952 |
ENST00000518824.5 | hg19 | chr6 | 43,738,984 | 43,752,395 | 13,412 |
ENST00000523125.5 | hg19 | chr6 | 43,738,984 | 43,752,299 | 13,316 |
ENST00000457104.6 | hg19 | chr6 | 43,738,984 | 43,752,299 | 13,316 |
ENST00000518689.5 | hg19 | chr6 | 43,738,984 | 43,752,299 | 13,316 |
ENST00000520948.5 | hg19 | chr6 | 43,738,820 | 43,752,686 | 13,867 |
ENST00000523873.5 | hg19 | chr6 | 43,738,946 | 43,752,346 | 13,401 |
ENST00000523950.5 | hg19 | chr6 | 43,738,946 | 43,752,639 | 13,694 |
ENST00000672860.3 | hg19 | chr6 | 43,737,948 | 43,754,224 | 16,277 |
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