KLK12 kallikrein related peptidase 12
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 8 |
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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52 |
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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
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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 | KLK-L5 |
SYNONYM | KLKL5 |
MIM | 605539 OMIM |
HGNC | HGNC:6360 HGNC |
Ensembl | ENSG00000186474 Ensembl |
AllianceGenome | HGNC:6360 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000684732.1 | hg38 | chr19 | 51,029,094 | 51,035,002 | 5,909 |
ENST00000319590.8 | hg38 | chr19 | 51,029,092 | 51,034,892 | 5,801 |
ENST00000525263.5 | hg38 | chr19 | 51,029,092 | 51,034,741 | 5,650 |
ENST00000250351.4 | hg38 | chr19 | 51,029,155 | 51,034,892 | 5,738 |
ENST00000529888.5 | hg38 | chr19 | 51,029,130 | 51,034,862 | 5,733 |
ENST00000525263.5 | hg19 | chr19 | 51,532,348 | 51,537,997 | 5,650 |
ENST00000319590.8 | hg19 | chr19 | 51,532,348 | 51,538,148 | 5,801 |
ENST00000684732.1 | hg19 | chr19 | 51,532,350 | 51,538,258 | 5,909 |
ENST00000529888.5 | hg19 | chr19 | 51,532,386 | 51,538,118 | 5,733 |
ENST00000250351.4 | hg19 | chr19 | 51,532,411 | 51,538,148 | 5,738 |
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