CLEC10A C-type lectin domain containing 10A
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 24 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
30 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CD301 |
| SYNONYM | CLECSF13 |
| SYNONYM | CLECSF14 |
| SYNONYM | HML |
| SYNONYM | HML2 |
| SYNONYM | MGL |
| MIM | 605999 OMIM |
| HGNC | HGNC:16916 HGNC |
| Ensembl | ENSG00000132514 Ensembl |
| AllianceGenome | HGNC:16916 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000254868.8 | hg38 | chr17 | 7,074,537 | 7,080,307 | 5,771 |
| ENST00000571664.1 | hg38 | chr17 | 7,074,796 | 7,080,283 | 5,488 |
| ENST00000416562.7 | hg38 | chr17 | 7,074,537 | 7,080,251 | 5,715 |
| ENST00000576617.5 | hg38 | chr17 | 7,074,795 | 7,080,248 | 5,454 |
| ENST00000416562.7 | hg19 | chr17 | 6,977,856 | 6,983,570 | 5,715 |
| ENST00000254868.8 | hg19 | chr17 | 6,977,856 | 6,983,626 | 5,771 |
| ENST00000576617.5 | hg19 | chr17 | 6,978,114 | 6,983,567 | 5,454 |
| ENST00000571664.1 | hg19 | chr17 | 6,978,115 | 6,983,602 | 5,488 |
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