SLC7A6OS solute carrier family 7 member 6 opposite strand
Information
- Symbol
- SLC7A6OS
- Type
- protein-coding
- Description
- solute carrier family 7 member 6 opposite strand
- Entrez Gene ID
- 84138
- Genome
- hg19
- Position
- chr16:68,331,937-68,344,849
- Genome
- hg38
- Position
- chr16:68,298,034-68,310,946
- MIM
- 619192 OMIM
- HGNC
- HGNC:25807 HGNC
- Ensembl
- ENSG00000103061 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 12 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 44 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
58 |
 |
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 | |||||||||||
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | EPM12 |
| SYNONYM | Iwr1 |
| MIM | 619192 OMIM |
| HGNC | HGNC:25807 HGNC |
| Ensembl | ENSG00000103061 Ensembl |
| AllianceGenome | HGNC:25807 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000263997.11 | hg38 | chr16 | 68,298,034 | 68,310,946 | 12,913 |
| ENST00000263997.11 | hg19 | chr16 | 68,331,937 | 68,344,849 | 12,913 |
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