KRT25 keratin 25
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Benign | 0 | 32 |
Likely benign | 0 | 32 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
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0 |
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0 |
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18 |
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108 |
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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
[No Data.]
Locus Zoom
Variants
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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 |
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Target data | : |
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 | ARWH3 |
SYNONYM | KRT24IRS1 |
SYNONYM | KRT25A |
MIM | 616646 OMIM |
HGNC | HGNC:30839 HGNC |
Ensembl | ENSG00000204897 Ensembl |
AllianceGenome | HGNC:30839 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000312150.5 | hg38 | chr17 | 40,748,021 | 40,755,331 | 7,311 |
ENST00000312150.5 | hg19 | chr17 | 38,904,273 | 38,911,583 | 7,311 |
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