KLK14 kallikrein related peptidase 14
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
not provided | 1 | 0 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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2 |
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 |
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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SYNONYM | KLK-L6 |
MIM | 606135 OMIM |
HGNC | HGNC:6362 HGNC |
Ensembl | ENSG00000129437 Ensembl |
AllianceGenome | HGNC:6362 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000391802.1 | hg38 | chr19 | 51,077,897 | 51,084,245 | 6,349 |
ENST00000156499.7 | hg38 | chr19 | 51,077,495 | 51,084,245 | 6,751 |
ENST00000650543.2 | hg38 | chr19 | 51,077,897 | 51,082,887 | 4,991 |
ENST00000156499.7 | hg19 | chr19 | 51,580,752 | 51,587,502 | 6,751 |
ENST00000650543.2 | hg19 | chr19 | 51,581,154 | 51,586,144 | 4,991 |
ENST00000391802.1 | hg19 | chr19 | 51,581,154 | 51,587,502 | 6,349 |
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