CD79A CD79a molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 8 |
Likely pathogenic | 0 | 4 |
Benign | 0 | 12 |
Likely benign | 0 | 134 |
Conflicting classifications of pathogenicity | 0 | 8 |
not provided | 4 | 0 |
Uncertain significance | 0 | 142 |
Ranking
ClinVar | |
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0 |
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0 |
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36 |
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260 |
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2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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Variants
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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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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 | IGA |
SYNONYM | IGAlpha |
SYNONYM | MB-1 |
SYNONYM | MB1 |
MIM | 112205 OMIM |
HGNC | HGNC:1698 HGNC |
Ensembl | ENSG00000105369 Ensembl |
AllianceGenome | HGNC:1698 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000444740.2 | hg38 | chr19 | 41,877,305 | 41,880,980 | 3,676 |
ENST00000221972.8 | hg38 | chr19 | 41,877,279 | 41,881,372 | 4,094 |
ENST00000597454.2 | hg38 | chr19 | 41,877,280 | 41,880,980 | 3,701 |
ENST00000221972.8 | hg19 | chr19 | 42,381,349 | 42,385,439 | 4,091 |
ENST00000597454.2 | hg19 | chr19 | 42,381,350 | 42,385,047 | 3,698 |
ENST00000444740.2 | hg19 | chr19 | 42,381,375 | 42,385,047 | 3,673 |
Key | Value |
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strand | + |
start | 42,381,189 |
Gene Symbol | CD79A |
Entrez GeneId | 973 |
Chr Band | 19q13.2 |
end | 42,385,438 |
chr | chr19 |
Name | CD79a molecule, immunoglobulin-associated alpha |
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