SLC6A15 solute carrier family 6 member 15
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 36 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
42 |
 |
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 | NTT73 |
| SYNONYM | SBAT1 |
| SYNONYM | V7-3 |
| SYNONYM | hv7-3 |
| MIM | 607971 OMIM |
| HGNC | HGNC:13621 HGNC |
| Ensembl | ENSG00000072041 Ensembl |
| AllianceGenome | HGNC:13621 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000680714.1 | hg38 | chr12 | 84,880,264 | 84,912,799 | 32,536 |
| ENST00000680469.1 | hg38 | chr12 | 84,859,505 | 84,912,823 | 53,319 |
| ENST00000681106.1 | hg38 | chr12 | 84,859,505 | 84,913,016 | 53,512 |
| ENST00000680892.1 | hg38 | chr12 | 84,859,505 | 84,912,793 | 53,289 |
| ENST00000681281.1 | hg38 | chr12 | 84,882,347 | 84,912,770 | 30,424 |
| ENST00000450363.4 | hg38 | chr12 | 84,880,845 | 84,912,876 | 32,032 |
| ENST00000681721.1 | hg38 | chr12 | 84,859,505 | 84,913,629 | 54,125 |
| ENST00000552192.5 | hg38 | chr12 | 84,861,594 | 84,912,801 | 51,208 |
| ENST00000679453.1 | hg38 | chr12 | 84,880,891 | 84,912,743 | 31,853 |
| ENST00000680963.1 | hg38 | chr12 | 84,859,505 | 84,910,717 | 51,213 |
| ENST00000680379.1 | hg38 | chr12 | 84,860,835 | 84,892,120 | 31,286 |
| ENST00000681688.1 | hg38 | chr12 | 84,880,179 | 84,911,179 | 31,001 |
| ENST00000266682.10 | hg38 | chr12 | 84,859,491 | 84,912,799 | 53,309 |
| ENST00000266682.10 | hg19 | chr12 | 85,253,270 | 85,306,578 | 53,309 |
| ENST00000552192.5 | hg19 | chr12 | 85,255,373 | 85,306,580 | 51,208 |
| ENST00000450363.4 | hg19 | chr12 | 85,274,624 | 85,306,655 | 32,032 |
| ENST00000679453.1 | hg19 | chr12 | 85,274,670 | 85,306,522 | 31,853 |
| ENST00000680963.1 | hg19 | chr12 | 85,253,284 | 85,304,496 | 51,213 |
| ENST00000680892.1 | hg19 | chr12 | 85,253,284 | 85,306,572 | 53,289 |
| ENST00000680379.1 | hg19 | chr12 | 85,254,614 | 85,285,899 | 31,286 |
| ENST00000680714.1 | hg19 | chr12 | 85,274,043 | 85,306,578 | 32,536 |
| ENST00000680469.1 | hg19 | chr12 | 85,253,284 | 85,306,602 | 53,319 |
| ENST00000681106.1 | hg19 | chr12 | 85,253,284 | 85,306,795 | 53,512 |
| ENST00000681281.1 | hg19 | chr12 | 85,276,126 | 85,306,549 | 30,424 |
| ENST00000681688.1 | hg19 | chr12 | 85,273,958 | 85,304,958 | 31,001 |
| ENST00000681721.1 | hg19 | chr12 | 85,253,284 | 85,307,408 | 54,125 |
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