TMEM220 transmembrane protein 220
Information
- Symbol
- TMEM220
- Type
- protein-coding
- Description
- transmembrane protein 220
- Entrez Gene ID
- 388335
- Genome
- hg19
- Position
- chr17:10,616,612-10,633,340
- Genome
- hg38
- Position
- chr17:10,713,295-10,730,023
- HGNC
- HGNC:33757 HGNC
- Ensembl
- ENSG00000187824 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 6 |
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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28 |
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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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000578345.1 | hg38 | chr17 | 10,715,422 | 10,729,986 | 14,565 |
ENST00000341871.8 | hg38 | chr17 | 10,713,295 | 10,730,023 | 16,729 |
ENST00000455996.6 | hg38 | chr17 | 10,714,676 | 10,730,023 | 15,348 |
ENST00000341871.8 | hg19 | chr17 | 10,616,612 | 10,633,340 | 16,729 |
ENST00000455996.6 | hg19 | chr17 | 10,617,993 | 10,633,340 | 15,348 |
ENST00000578345.1 | hg19 | chr17 | 10,618,739 | 10,633,303 | 14,565 |
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