MS4A4E membrane spanning 4-domains A4E
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 5 | 0 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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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
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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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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MIM | 608401 OMIM |
HGNC | HGNC:14284 HGNC |
Ensembl | ENSG00000214787 Ensembl |
AllianceGenome | HGNC:14284 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000651255.1 | hg38 | chr11 | 60,200,270 | 60,243,137 | 42,868 |
ENST00000398984.6 | hg38 | chr11 | 60,213,089 | 60,230,055 | 16,967 |
ENST00000651255.1 | hg19 | chr11 | 59,967,743 | 60,010,610 | 42,868 |
ENST00000398984.6 | hg19 | chr11 | 59,980,562 | 59,997,528 | 16,967 |
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