LYPD6 LY6/PLAUR domain containing 6
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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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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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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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MIM | 613359 OMIM |
HGNC | HGNC:28751 HGNC |
Ensembl | ENSG00000187123 Ensembl |
AllianceGenome | HGNC:28751 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000334166.9 | hg38 | chr2 | 149,330,587 | 149,474,138 | 143,552 |
ENST00000409381.5 | hg38 | chr2 | 149,329,985 | 149,473,623 | 143,639 |
ENST00000651933.1 | hg38 | chr2 | 149,367,701 | 149,471,107 | 103,407 |
ENST00000409381.5 | hg19 | chr2 | 150,186,499 | 150,330,137 | 143,639 |
ENST00000334166.9 | hg19 | chr2 | 150,187,101 | 150,330,652 | 143,552 |
ENST00000651933.1 | hg19 | chr2 | 150,224,215 | 150,327,621 | 103,407 |
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