SCYL1 SCY1 like pseudokinase 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 30 |
Likely pathogenic | 0 | 14 |
Benign | 0 | 40 |
Likely benign | 0 | 100 |
Conflicting classifications of pathogenicity | 0 | 4 |
Uncertain significance | 0 | 124 |
Ranking
ClinVar | |
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0 |
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0 |
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56 |
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214 |
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16 |
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 |
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 | GKLP |
SYNONYM | HT019 |
SYNONYM | NKTL |
SYNONYM | NTKL |
SYNONYM | P105 |
SYNONYM | SCAR21 |
SYNONYM | TAPK |
SYNONYM | TEIF |
SYNONYM | TRAP |
MIM | 607982 OMIM |
HGNC | HGNC:14372 HGNC |
Ensembl | ENSG00000142186 Ensembl |
AllianceGenome | HGNC:14372 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000527009.5 | hg38 | chr11 | 65,525,413 | 65,538,675 | 13,263 |
ENST00000533862.5 | hg38 | chr11 | 65,525,112 | 65,538,704 | 13,593 |
ENST00000270176.10 | hg38 | chr11 | 65,525,083 | 65,538,704 | 13,622 |
ENST00000524944.5 | hg38 | chr11 | 65,525,121 | 65,538,704 | 13,584 |
ENST00000420247.6 | hg38 | chr11 | 65,525,085 | 65,538,704 | 13,620 |
ENST00000525364.5 | hg38 | chr11 | 65,525,077 | 65,538,704 | 13,628 |
ENST00000525364.5 | hg19 | chr11 | 65,292,548 | 65,306,175 | 13,628 |
ENST00000270176.10 | hg19 | chr11 | 65,292,554 | 65,306,175 | 13,622 |
ENST00000420247.6 | hg19 | chr11 | 65,292,556 | 65,306,175 | 13,620 |
ENST00000533862.5 | hg19 | chr11 | 65,292,583 | 65,306,175 | 13,593 |
ENST00000524944.5 | hg19 | chr11 | 65,292,592 | 65,306,175 | 13,584 |
ENST00000527009.5 | hg19 | chr11 | 65,292,884 | 65,306,146 | 13,263 |
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