FASTKD5 FAST kinase domains 5
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 10 |
Uncertain significance | 0 | 86 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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96 |
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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
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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Target data | : |
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 | dJ1187M17.5 |
MIM | 614272 OMIM |
HGNC | HGNC:25790 HGNC |
Ensembl | ENSG00000215251 Ensembl |
AllianceGenome | HGNC:25790 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000380266.4 | hg38 | chr20 | 3,146,519 | 3,159,865 | 13,347 |
ENST00000687419.1 | hg38 | chr20 | 3,146,537 | 3,159,853 | 13,317 |
ENST00000692371.1 | hg38 | chr20 | 3,146,523 | 3,159,795 | 13,273 |
ENST00000688674.1 | hg38 | chr20 | 3,146,539 | 3,159,865 | 13,327 |
ENST00000380266.4 | hg19 | chr20 | 3,127,165 | 3,140,511 | 13,347 |
ENST00000692371.1 | hg19 | chr20 | 3,127,169 | 3,140,441 | 13,273 |
ENST00000687419.1 | hg19 | chr20 | 3,127,183 | 3,140,499 | 13,317 |
ENST00000688674.1 | hg19 | chr20 | 3,127,185 | 3,140,511 | 13,327 |
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