KLK6 kallikrein related peptidase 6
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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
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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 | Bssp |
SYNONYM | Klk7 |
SYNONYM | PRSS18 |
SYNONYM | PRSS9 |
SYNONYM | SP59 |
SYNONYM | hK6 |
MIM | 602652 OMIM |
HGNC | HGNC:6367 HGNC |
Ensembl | ENSG00000167755 Ensembl |
AllianceGenome | HGNC:6367 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000391808.5 | hg38 | chr19 | 50,958,632 | 50,968,791 | 10,160 |
ENST00000310157.7 | hg38 | chr19 | 50,958,631 | 50,969,591 | 10,961 |
ENST00000594641.1 | hg38 | chr19 | 50,959,149 | 50,968,196 | 9,048 |
ENST00000376851.7 | hg38 | chr19 | 50,958,631 | 50,968,972 | 10,342 |
ENST00000376851.7 | hg19 | chr19 | 51,461,887 | 51,472,228 | 10,342 |
ENST00000310157.7 | hg19 | chr19 | 51,461,887 | 51,472,847 | 10,961 |
ENST00000391808.5 | hg19 | chr19 | 51,461,888 | 51,472,047 | 10,160 |
ENST00000594641.1 | hg19 | chr19 | 51,462,405 | 51,471,452 | 9,048 |
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