CARD16 caspase recruitment domain family member 16
Information
- Symbol
- CARD16
- Type
- protein-coding
- Description
- caspase recruitment domain family member 16
- Entrez Gene ID
- 114769
- Genome
- hg19
- Position
- chr11:104,912,290-104,916,062
- Genome
- hg38
- Position
- chr11:105,041,563-105,045,335
- MIM
- 615680 OMIM
- HGNC
- HGNC:33701 HGNC
- Ensembl
- ENSG00000204397 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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36 |
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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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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 |
---|---|
SYNONYM | COP |
SYNONYM | COP1 |
SYNONYM | LLID-114769 |
SYNONYM | PSEUDO-ICE |
MIM | 615680 OMIM |
HGNC | HGNC:33701 HGNC |
Ensembl | ENSG00000204397 Ensembl |
AllianceGenome | HGNC:33701 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000673097.2 | hg38 | chr11 | 105,041,563 | 105,045,335 | 3,773 |
ENST00000672037.1 | hg38 | chr11 | 105,041,326 | 105,045,315 | 3,990 |
ENST00000672037.1 | hg19 | chr11 | 104,912,053 | 104,916,042 | 3,990 |
ENST00000673097.2 | hg19 | chr11 | 104,912,290 | 104,916,062 | 3,773 |
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