KRT73 keratin 73
Clinical Significance
MGeND | ClinVar | |
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Likely benign | 0 | 2 |
Uncertain significance | 0 | 88 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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90 |
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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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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 |
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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 | CK-73 |
SYNONYM | IRT6IRS3 |
SYNONYM | K6IRS3 |
SYNONYM | K73 |
SYNONYM | KRT6IRS3 |
MIM | 608247 OMIM |
HGNC | HGNC:28928 HGNC |
Ensembl | ENSG00000186049 Ensembl |
AllianceGenome | HGNC:28928 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000305748.7 | hg38 | chr12 | 52,607,570 | 52,618,559 | 10,990 |
ENST00000305748.7 | hg19 | chr12 | 53,001,354 | 53,012,343 | 10,990 |
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