CD22 CD22 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 18 |
Uncertain significance | 0 | 92 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
118 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
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
|
Category | : |
|
Search word | : | |
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 | SIGLEC-2 |
SYNONYM | SIGLEC2 |
MIM | 107266 OMIM |
HGNC | HGNC:1643 HGNC |
Ensembl | ENSG00000012124 Ensembl |
AllianceGenome | HGNC:1643 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000594250.5 | hg38 | chr19 | 35,332,016 | 35,346,766 | 14,751 |
ENST00000341773.10 | hg38 | chr19 | 35,329,169 | 35,347,355 | 18,187 |
ENST00000544992.6 | hg38 | chr19 | 35,329,212 | 35,346,929 | 17,718 |
ENST00000536635.6 | hg38 | chr19 | 35,329,187 | 35,347,355 | 18,169 |
ENST00000419549.6 | hg38 | chr19 | 35,329,212 | 35,346,929 | 17,718 |
ENST00000085219.10 | hg38 | chr19 | 35,329,187 | 35,347,361 | 18,175 |
ENST00000085219.10 | hg19 | chr19 | 35,820,090 | 35,838,264 | 18,175 |
ENST00000341773.10 | hg19 | chr19 | 35,820,072 | 35,838,258 | 18,187 |
ENST00000544992.6 | hg19 | chr19 | 35,820,115 | 35,837,832 | 17,718 |
ENST00000419549.6 | hg19 | chr19 | 35,820,115 | 35,837,832 | 17,718 |
ENST00000594250.5 | hg19 | chr19 | 35,822,919 | 35,837,669 | 14,751 |
ENST00000536635.6 | hg19 | chr19 | 35,820,090 | 35,838,258 | 18,169 |
Genome browser