CENPL centromere protein L
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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48 |
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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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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 | C1orf155 |
SYNONYM | CENP-L |
SYNONYM | dJ383J4.3 |
MIM | 611503 OMIM |
HGNC | HGNC:17879 HGNC |
Ensembl | ENSG00000120334 Ensembl |
AllianceGenome | HGNC:17879 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000345664.10 | hg38 | chr1 | 173,799,850 | 173,824,132 | 24,283 |
ENST00000356198.6 | hg38 | chr1 | 173,799,550 | 173,824,322 | 24,773 |
ENST00000367710.7 | hg38 | chr1 | 173,799,850 | 173,824,174 | 24,325 |
ENST00000682279.1 | hg38 | chr1 | 173,799,550 | 173,824,883 | 25,334 |
ENST00000356198.6 | hg19 | chr1 | 173,768,688 | 173,793,460 | 24,773 |
ENST00000682279.1 | hg19 | chr1 | 173,768,688 | 173,794,021 | 25,334 |
ENST00000345664.10 | hg19 | chr1 | 173,768,988 | 173,793,270 | 24,283 |
ENST00000367710.7 | hg19 | chr1 | 173,768,988 | 173,793,312 | 24,325 |
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