TMEM204 transmembrane protein 204
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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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 | C16orf30 |
SYNONYM | CLP24 |
MIM | 611002 OMIM |
HGNC | HGNC:14158 HGNC |
Ensembl | ENSG00000131634 Ensembl |
AllianceGenome | HGNC:14158 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000253934.9 | hg38 | chr16 | 1,528,688 | 1,555,580 | 26,893 |
ENST00000566264.2 | hg38 | chr16 | 1,533,666 | 1,555,568 | 21,903 |
ENST00000253934.9 | hg19 | chr16 | 1,578,689 | 1,605,581 | 26,893 |
ENST00000566264.2 | hg19 | chr16 | 1,583,667 | 1,605,569 | 21,903 |
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