SLC5A10 solute carrier family 5 member 10
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 20 |
not provided | 2 | 0 |
Uncertain significance | 0 | 210 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
232 |
![]() |
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
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 | SGLT-5 |
SYNONYM | SGLT5 |
MIM | 618636 OMIM |
HGNC | HGNC:23155 HGNC |
Ensembl | ENSG00000154025 Ensembl |
AllianceGenome | HGNC:23155 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000317977.10 | hg38 | chr17 | 18,950,345 | 19,022,595 | 72,251 |
ENST00000395645.4 | hg38 | chr17 | 18,952,165 | 19,022,565 | 70,401 |
ENST00000395647.6 | hg38 | chr17 | 18,952,165 | 19,020,691 | 68,527 |
ENST00000395643.6 | hg38 | chr17 | 18,952,188 | 19,020,685 | 68,498 |
ENST00000417251.6 | hg38 | chr17 | 18,952,165 | 19,020,691 | 68,527 |
ENST00000317977.10 | hg19 | chr17 | 18,853,658 | 18,925,908 | 72,251 |
ENST00000395647.6 | hg19 | chr17 | 18,855,478 | 18,924,004 | 68,527 |
ENST00000417251.6 | hg19 | chr17 | 18,855,478 | 18,924,004 | 68,527 |
ENST00000395645.4 | hg19 | chr17 | 18,855,478 | 18,925,878 | 70,401 |
ENST00000395643.6 | hg19 | chr17 | 18,855,501 | 18,923,998 | 68,498 |
Genome browser