TMEM208 transmembrane protein 208
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 20 |
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
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 |
Search Word
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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Filtering | : |
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 | HSPC171 |
SYNONYM | SND2 |
SYNONYM | hSND2 |
MIM | 620781 OMIM |
HGNC | HGNC:25015 HGNC |
Ensembl | ENSG00000168701 Ensembl |
AllianceGenome | HGNC:25015 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000304800.14 | hg38 | chr16 | 67,227,130 | 67,229,278 | 2,149 |
ENST00000563953.5 | hg38 | chr16 | 67,227,120 | 67,229,262 | 2,143 |
ENST00000565201.1 | hg38 | chr16 | 67,227,168 | 67,229,278 | 2,111 |
ENST00000563953.5 | hg19 | chr16 | 67,261,023 | 67,263,165 | 2,143 |
ENST00000304800.14 | hg19 | chr16 | 67,261,033 | 67,263,181 | 2,149 |
ENST00000565201.1 | hg19 | chr16 | 67,261,071 | 67,263,181 | 2,111 |
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