TMEM259 transmembrane protein 259
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 102 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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110 |
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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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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 | ASBABP1 |
SYNONYM | C19orf6 |
SYNONYM | MBRL |
SYNONYM | MEMBRALIN |
SYNONYM | R32184_3 |
MIM | 611011 OMIM |
HGNC | HGNC:17039 HGNC |
Ensembl | ENSG00000182087 Ensembl |
AllianceGenome | HGNC:17039 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000592590.6 | hg38 | chr19 | 1,009,650 | 1,017,420 | 7,771 |
ENST00000333175.9 | hg38 | chr19 | 1,009,651 | 1,021,115 | 11,465 |
ENST00000356663.8 | hg38 | chr19 | 1,009,653 | 1,021,123 | 11,471 |
ENST00000592590.6 | hg19 | chr19 | 1,009,649 | 1,017,419 | 7,771 |
ENST00000333175.9 | hg19 | chr19 | 1,009,650 | 1,021,114 | 11,465 |
ENST00000356663.8 | hg19 | chr19 | 1,009,652 | 1,021,122 | 11,471 |
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