LCE2B late cornified envelope 2B
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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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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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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 | LEP10 |
SYNONYM | SPRL1B |
SYNONYM | XP5 |
MIM | 612610 OMIM |
HGNC | HGNC:16610 HGNC |
Ensembl | ENSG00000159455 Ensembl |
AllianceGenome | HGNC:16610 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000368780.4 | hg38 | chr1 | 152,686,123 | 152,687,397 | 1,275 |
ENST00000368780.4 | hg19 | chr1 | 152,658,599 | 152,659,873 | 1,275 |
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