MLN motilin
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 4 | 0 |
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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8 |
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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 |
Search Word
Target data | : |
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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Category | : |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000507738.1 | hg38 | chr6 | 33,794,787 | 33,803,980 | 9,194 |
ENST00000266003.9 | hg38 | chr6 | 33,794,700 | 33,804,002 | 9,303 |
ENST00000430124.7 | hg38 | chr6 | 33,794,673 | 33,804,003 | 9,331 |
ENST00000430124.7 | hg19 | chr6 | 33,762,450 | 33,771,780 | 9,331 |
ENST00000266003.9 | hg19 | chr6 | 33,762,477 | 33,771,779 | 9,303 |
ENST00000507738.1 | hg19 | chr6 | 33,762,564 | 33,771,757 | 9,194 |
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