LYZ lysozyme
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 10 |
Benign | 0 | 34 |
Likely benign | 0 | 14 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 72 |
Ranking
ClinVar | |
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0 |
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0 |
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16 |
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106 |
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6 |
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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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 | AMYLD5 |
SYNONYM | LYZF1 |
SYNONYM | LZM |
MIM | 153450 OMIM |
HGNC | HGNC:6740 HGNC |
Ensembl | ENSG00000090382 Ensembl |
AllianceGenome | HGNC:6740 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000548839.1 | hg38 | chr12 | 69,348,386 | 69,350,506 | 2,121 |
ENST00000261267.7 | hg38 | chr12 | 69,348,381 | 69,354,234 | 5,854 |
ENST00000549690.1 | hg38 | chr12 | 69,348,384 | 69,353,495 | 5,112 |
ENST00000261267.7 | hg19 | chr12 | 69,742,161 | 69,748,014 | 5,854 |
ENST00000549690.1 | hg19 | chr12 | 69,742,164 | 69,747,275 | 5,112 |
ENST00000548839.1 | hg19 | chr12 | 69,742,166 | 69,744,286 | 2,121 |
Key | Value |
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strand | + |
start | 69,742,133 |
Gene Symbol | LYZ |
Entrez GeneId | 4,069 |
Chr Band | 12q15 |
end | 69,748,012 |
chr | chr12 |
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