C1QB complement C1q B chain
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 2 | 6 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 26 |
Likely benign | 0 | 76 |
Uncertain significance | 0 | 88 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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26 |
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164 |
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6 |
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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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 | C1QD2 |
MIM | 120570 OMIM |
HGNC | HGNC:1242 HGNC |
Ensembl | ENSG00000173369 Ensembl |
AllianceGenome | HGNC:1242 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000695758.1 | hg38 | chr1 | 22,653,190 | 22,661,535 | 8,346 |
ENST00000695759.1 | hg38 | chr1 | 22,653,190 | 22,661,535 | 8,346 |
ENST00000695756.1 | hg38 | chr1 | 22,653,190 | 22,661,535 | 8,346 |
ENST00000695755.1 | hg38 | chr1 | 22,653,190 | 22,661,535 | 8,346 |
ENST00000695757.1 | hg38 | chr1 | 22,653,190 | 22,661,535 | 8,346 |
ENST00000695754.1 | hg38 | chr1 | 22,653,190 | 22,661,535 | 8,346 |
ENST00000695760.1 | hg38 | chr1 | 22,653,190 | 22,661,535 | 8,346 |
ENST00000695761.1 | hg38 | chr1 | 22,653,190 | 22,661,535 | 8,346 |
ENST00000509305.6 | hg38 | chr1 | 22,653,236 | 22,661,637 | 8,402 |
ENST00000695762.1 | hg38 | chr1 | 22,653,203 | 22,661,535 | 8,333 |
ENST00000695763.1 | hg38 | chr1 | 22,659,399 | 22,661,535 | 2,137 |
ENST00000695754.1 | hg19 | chr1 | 22,979,683 | 22,988,028 | 8,346 |
ENST00000695755.1 | hg19 | chr1 | 22,979,683 | 22,988,028 | 8,346 |
ENST00000695756.1 | hg19 | chr1 | 22,979,683 | 22,988,028 | 8,346 |
ENST00000695757.1 | hg19 | chr1 | 22,979,683 | 22,988,028 | 8,346 |
ENST00000695758.1 | hg19 | chr1 | 22,979,683 | 22,988,028 | 8,346 |
ENST00000695759.1 | hg19 | chr1 | 22,979,683 | 22,988,028 | 8,346 |
ENST00000695760.1 | hg19 | chr1 | 22,979,683 | 22,988,028 | 8,346 |
ENST00000695761.1 | hg19 | chr1 | 22,979,683 | 22,988,028 | 8,346 |
ENST00000695762.1 | hg19 | chr1 | 22,979,696 | 22,988,028 | 8,333 |
ENST00000509305.6 | hg19 | chr1 | 22,979,729 | 22,988,130 | 8,402 |
ENST00000695763.1 | hg19 | chr1 | 22,985,892 | 22,988,028 | 2,137 |
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