SLC35B2 solute carrier family 35 member B2
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 2 |
| Benign | 0 | 4 |
| Likely benign | 0 | 8 |
| Uncertain significance | 0 | 72 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
84 |
 |
2 |
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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| 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 | HLD26 |
| SYNONYM | PAPST1 |
| SYNONYM | SLL |
| SYNONYM | UGTrel4 |
| MIM | 610788 OMIM |
| HGNC | HGNC:16872 HGNC |
| Ensembl | ENSG00000157593 Ensembl |
| AllianceGenome | HGNC:16872 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000538577.5 | hg38 | chr6 | 44,254,102 | 44,257,571 | 3,470 |
| ENST00000615337.4 | hg38 | chr6 | 44,254,102 | 44,257,890 | 3,789 |
| ENST00000393810.5 | hg38 | chr6 | 44,254,096 | 44,257,554 | 3,459 |
| ENST00000393812.4 | hg38 | chr6 | 44,254,101 | 44,257,528 | 3,428 |
| ENST00000537814.2 | hg38 | chr6 | 44,254,102 | 44,257,571 | 3,470 |
| ENST00000393810.5 | hg19 | chr6 | 44,221,833 | 44,225,291 | 3,459 |
| ENST00000393812.4 | hg19 | chr6 | 44,221,838 | 44,225,265 | 3,428 |
| ENST00000537814.2 | hg19 | chr6 | 44,221,839 | 44,225,308 | 3,470 |
| ENST00000538577.5 | hg19 | chr6 | 44,221,839 | 44,225,308 | 3,470 |
| ENST00000615337.4 | hg19 | chr6 | 44,221,839 | 44,225,627 | 3,789 |
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