LYPD5 LY6/PLAUR domain containing 5
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
not provided | 1 | 0 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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32 |
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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
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 | HALDISIN |
SYNONYM | PRO4356 |
MIM | 619618 OMIM |
HGNC | HGNC:26397 HGNC |
Ensembl | ENSG00000159871 Ensembl |
AllianceGenome | HGNC:26397 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000594013.5 | hg38 | chr19 | 43,796,959 | 43,800,029 | 3,071 |
ENST00000377950.8 | hg38 | chr19 | 43,795,927 | 43,802,447 | 6,521 |
ENST00000414615.6 | hg38 | chr19 | 43,796,241 | 43,820,634 | 24,394 |
ENST00000377950.8 | hg19 | chr19 | 44,300,079 | 44,306,599 | 6,521 |
ENST00000414615.6 | hg19 | chr19 | 44,300,393 | 44,324,786 | 24,394 |
ENST00000594013.5 | hg19 | chr19 | 44,301,111 | 44,304,181 | 3,071 |
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