CYLC1 cylicin 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely benign | 0 | 16 |
not provided | 6 | 0 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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68 |
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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
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 | CYCL1 |
SYNONYM | SPGFX8 |
MIM | 300768 OMIM |
HGNC | HGNC:2582 HGNC |
Ensembl | ENSG00000183035 Ensembl |
AllianceGenome | HGNC:2582 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000621735.4 | hg38 | chrX | 83,861,126 | 83,886,699 | 25,574 |
ENST00000329312.5 | hg38 | chrX | 83,861,146 | 83,886,698 | 25,553 |
ENST00000621735.4 | hg19 | chrX | 83,116,134 | 83,141,707 | 25,574 |
ENST00000329312.5 | hg19 | chrX | 83,116,154 | 83,141,706 | 25,553 |
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