ECM2 extracellular matrix protein 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 82 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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86 |
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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
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 |
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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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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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ENST00000344604.10 | hg38 | chr9 | 92,495,315 | 92,535,990 | 40,676 |
ENST00000444490.6 | hg38 | chr9 | 92,493,554 | 92,536,092 | 42,539 |
ENST00000375540.5 | hg38 | chr9 | 92,516,712 | 92,536,055 | 19,344 |
ENST00000444490.6 | hg19 | chr9 | 95,255,836 | 95,298,374 | 42,539 |
ENST00000344604.10 | hg19 | chr9 | 95,257,597 | 95,298,272 | 40,676 |
ENST00000375540.5 | hg19 | chr9 | 95,278,994 | 95,298,337 | 19,344 |
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