MUC21 mucin 21, cell surface associated
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 96 |
not provided | 2 | 0 |
Uncertain significance | 0 | 66 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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164 |
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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
Locus Zoom
Variants
Search Word
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 |
Search Word
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 | C6orf205 |
SYNONYM | KMQK697 |
SYNONYM | MUC-21 |
MIM | 616991 OMIM |
HGNC | HGNC:21661 HGNC |
Ensembl | ENSG00000204544 Ensembl |
AllianceGenome | HGNC:21661 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000376296.3 | hg38 | chr6 | 30,983,718 | 30,989,903 | 6,186 |
ENST00000486149.2 | hg38 | chr6 | 30,983,718 | 30,988,637 | 4,920 |
ENST00000486149.2 | hg19 | chr6 | 30,951,495 | 30,956,414 | 4,920 |
ENST00000376296.3 | hg19 | chr6 | 30,951,495 | 30,957,680 | 6,186 |
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