CD209 CD209 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 16 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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52 |
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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
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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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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 | CDSIGN |
SYNONYM | CLEC4L |
SYNONYM | DC-SIGN |
SYNONYM | DC-SIGN1 |
SYNONYM | hDC-SIGN |
MIM | 604672 OMIM |
HGNC | HGNC:1641 HGNC |
Ensembl | ENSG00000090659 Ensembl |
AllianceGenome | HGNC:1641 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000315599.12 | hg38 | chr19 | 7,739,993 | 7,747,534 | 7,542 |
ENST00000204801.12 | hg38 | chr19 | 7,743,039 | 7,747,511 | 4,473 |
ENST00000394173.8 | hg38 | chr19 | 7,742,511 | 7,747,564 | 5,054 |
ENST00000354397.10 | hg38 | chr19 | 7,743,039 | 7,747,511 | 4,473 |
ENST00000315591.12 | hg38 | chr19 | 7,743,039 | 7,747,511 | 4,473 |
ENST00000593660.5 | hg38 | chr19 | 7,742,647 | 7,747,511 | 4,865 |
ENST00000394161.9 | hg38 | chr19 | 7,743,039 | 7,747,511 | 4,473 |
ENST00000601951.5 | hg38 | chr19 | 7,742,850 | 7,747,518 | 4,669 |
ENST00000593821.5 | hg38 | chr19 | 7,743,039 | 7,747,511 | 4,473 |
ENST00000601256.1 | hg38 | chr19 | 7,743,175 | 7,747,511 | 4,337 |
ENST00000602261.5 | hg38 | chr19 | 7,743,039 | 7,747,511 | 4,473 |
ENST00000315599.12 | hg19 | chr19 | 7,804,879 | 7,812,420 | 7,542 |
ENST00000394173.8 | hg19 | chr19 | 7,807,397 | 7,812,450 | 5,054 |
ENST00000593660.5 | hg19 | chr19 | 7,807,533 | 7,812,397 | 4,865 |
ENST00000601951.5 | hg19 | chr19 | 7,807,736 | 7,812,404 | 4,669 |
ENST00000204801.12 | hg19 | chr19 | 7,807,925 | 7,812,397 | 4,473 |
ENST00000315591.12 | hg19 | chr19 | 7,807,925 | 7,812,397 | 4,473 |
ENST00000354397.10 | hg19 | chr19 | 7,807,925 | 7,812,397 | 4,473 |
ENST00000394161.9 | hg19 | chr19 | 7,807,925 | 7,812,397 | 4,473 |
ENST00000593821.5 | hg19 | chr19 | 7,807,925 | 7,812,397 | 4,473 |
ENST00000602261.5 | hg19 | chr19 | 7,807,925 | 7,812,397 | 4,473 |
ENST00000601256.1 | hg19 | chr19 | 7,808,061 | 7,812,397 | 4,337 |
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