SLC25A51 solute carrier family 25 member 51
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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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
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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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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 |
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Target data | : |
MGeND data only
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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 | CG7943 |
SYNONYM | MCART1 |
MIM | 619153 OMIM |
HGNC | HGNC:23323 HGNC |
Ensembl | ENSG00000122696 Ensembl |
AllianceGenome | HGNC:23323 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000242275.7 | hg38 | chr9 | 37,887,604 | 37,904,127 | 16,524 |
ENST00000377716.6 | hg38 | chr9 | 37,887,604 | 37,904,110 | 16,507 |
ENST00000377716.6 | hg19 | chr9 | 37,887,601 | 37,904,107 | 16,507 |
ENST00000242275.7 | hg19 | chr9 | 37,887,601 | 37,904,124 | 16,524 |
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