YKT6 YKT6 v-SNARE homolog
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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
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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MIM | 606209 OMIM |
HGNC | HGNC:16959 HGNC |
Ensembl | ENSG00000106636 Ensembl |
AllianceGenome | HGNC:16959 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000677090.1 | hg38 | chr7 | 44,201,012 | 44,212,595 | 11,584 |
ENST00000496112.5 | hg38 | chr7 | 44,200,968 | 44,212,889 | 11,922 |
ENST00000678359.1 | hg38 | chr7 | 44,200,972 | 44,214,259 | 13,288 |
ENST00000223369.3 | hg38 | chr7 | 44,200,978 | 44,214,294 | 13,317 |
ENST00000496112.5 | hg19 | chr7 | 44,240,567 | 44,252,488 | 11,922 |
ENST00000678359.1 | hg19 | chr7 | 44,240,571 | 44,253,858 | 13,288 |
ENST00000223369.3 | hg19 | chr7 | 44,240,577 | 44,253,893 | 13,317 |
ENST00000677090.1 | hg19 | chr7 | 44,240,611 | 44,252,194 | 11,584 |
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