SLC16A5 solute carrier family 16 member 5
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 68 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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74 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | MCT5 |
SYNONYM | MCT6 |
MIM | 603879 OMIM |
HGNC | HGNC:10926 HGNC |
Ensembl | ENSG00000170190 Ensembl |
AllianceGenome | HGNC:10926 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000450736.6 | hg38 | chr17 | 75,088,938 | 75,106,151 | 17,214 |
ENST00000538213.6 | hg38 | chr17 | 75,093,287 | 75,104,410 | 11,124 |
ENST00000329783.9 | hg38 | chr17 | 75,087,954 | 75,106,162 | 18,209 |
ENST00000580123.5 | hg38 | chr17 | 75,087,727 | 75,106,162 | 18,436 |
ENST00000580123.5 | hg19 | chr17 | 73,083,822 | 73,102,257 | 18,436 |
ENST00000329783.9 | hg19 | chr17 | 73,084,049 | 73,102,257 | 18,209 |
ENST00000450736.6 | hg19 | chr17 | 73,085,033 | 73,102,246 | 17,214 |
ENST00000538213.6 | hg19 | chr17 | 73,089,382 | 73,100,505 | 11,124 |
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