TMEM79 transmembrane protein 79
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 78 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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94 |
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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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Search word | : | |
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 | MATT |
MIM | 615531 OMIM |
HGNC | HGNC:28196 HGNC |
Ensembl | ENSG00000163472 Ensembl |
AllianceGenome | HGNC:28196 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000405535.3 | hg38 | chr1 | 156,284,325 | 156,292,443 | 8,119 |
ENST00000295694.9 | hg38 | chr1 | 156,282,948 | 156,292,443 | 9,496 |
ENST00000357501.6 | hg38 | chr1 | 156,282,953 | 156,291,948 | 8,996 |
ENST00000295694.9 | hg19 | chr1 | 156,252,739 | 156,262,234 | 9,496 |
ENST00000357501.6 | hg19 | chr1 | 156,252,744 | 156,261,739 | 8,996 |
ENST00000405535.3 | hg19 | chr1 | 156,254,116 | 156,262,234 | 8,119 |
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