NEU3 neuraminidase 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 84 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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88 |
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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 | SIAL3 |
MIM | 604617 OMIM |
HGNC | HGNC:7760 HGNC |
Ensembl | ENSG00000162139 Ensembl |
AllianceGenome | HGNC:7760 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000531509.5 | hg38 | chr11 | 74,988,279 | 75,007,084 | 18,806 |
ENST00000294064.9 | hg38 | chr11 | 74,988,933 | 75,010,907 | 21,975 |
ENST00000532963.1 | hg38 | chr11 | 74,988,934 | 75,006,834 | 17,901 |
ENST00000534628.1 | hg38 | chr11 | 74,988,944 | 74,995,043 | 6,100 |
ENST00000531619.1 | hg38 | chr11 | 74,988,943 | 75,005,469 | 16,527 |
ENST00000526068.1 | hg38 | chr11 | 74,988,925 | 74,990,163 | 1,239 |
ENST00000529024.1 | hg38 | chr11 | 74,988,698 | 75,018,893 | 30,196 |
ENST00000531509.5 | hg19 | chr11 | 74,699,324 | 74,718,129 | 18,806 |
ENST00000529024.1 | hg19 | chr11 | 74,699,743 | 74,729,938 | 30,196 |
ENST00000526068.1 | hg19 | chr11 | 74,699,970 | 74,701,208 | 1,239 |
ENST00000294064.9 | hg19 | chr11 | 74,699,978 | 74,721,952 | 21,975 |
ENST00000532963.1 | hg19 | chr11 | 74,699,979 | 74,717,879 | 17,901 |
ENST00000531619.1 | hg19 | chr11 | 74,699,988 | 74,716,514 | 16,527 |
ENST00000534628.1 | hg19 | chr11 | 74,699,989 | 74,706,088 | 6,100 |
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