TLR7 toll like receptor 7
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 8 |
Benign | 0 | 34 |
Likely benign | 0 | 148 |
Conflicting classifications of pathogenicity | 0 | 2 |
not provided | 7 | 0 |
Uncertain significance | 0 | 216 |
Ranking
ClinVar | |
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0 |
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0 |
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24 |
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368 |
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8 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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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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 | IMD74 |
SYNONYM | SLEB17 |
SYNONYM | TLR7-like |
MIM | 300365 OMIM |
HGNC | HGNC:15631 HGNC |
Ensembl | ENSG00000196664 Ensembl |
AllianceGenome | HGNC:15631 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000380659.4 | hg38 | chrX | 12,867,072 | 12,890,361 | 23,290 |
ENST00000380659.4 | hg19 | chrX | 12,885,191 | 12,908,480 | 23,290 |
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