SORT1 sortilin 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 16 |
Likely benign | 0 | 16 |
not provided | 1 | 0 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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72 |
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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
Locus Zoom
Variants
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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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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 | Gp95 |
SYNONYM | LDLCQ6 |
SYNONYM | NT3 |
SYNONYM | NTR3 |
MIM | 602458 OMIM |
HGNC | HGNC:11186 HGNC |
Ensembl | ENSG00000134243 Ensembl |
AllianceGenome | HGNC:11186 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000256637.8 | hg38 | chr1 | 109,309,575 | 109,397,918 | 88,344 |
ENST00000538502.5 | hg38 | chr1 | 109,309,568 | 109,393,357 | 83,790 |
ENST00000538502.5 | hg19 | chr1 | 109,852,190 | 109,935,979 | 83,790 |
ENST00000256637.8 | hg19 | chr1 | 109,852,197 | 109,940,540 | 88,344 |
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