YIPF2 Yip1 domain family member 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 10 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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56 |
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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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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 |
Type | ID |
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SYNONYM | FinGER2 |
SYNONYM | YIPFbeta3B |
SYNONYM | Yip5C |
MIM | 617522 OMIM |
HGNC | HGNC:28476 HGNC |
Ensembl | ENSG00000130733 Ensembl |
AllianceGenome | HGNC:28476 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000586748.6 | hg38 | chr19 | 10,922,193 | 10,928,639 | 6,447 |
ENST00000253031.6 | hg38 | chr19 | 10,922,185 | 10,928,681 | 6,497 |
ENST00000590329.5 | hg38 | chr19 | 10,923,272 | 10,928,585 | 5,314 |
ENST00000253031.6 | hg19 | chr19 | 11,032,861 | 11,039,357 | 6,497 |
ENST00000586748.6 | hg19 | chr19 | 11,032,869 | 11,039,315 | 6,447 |
ENST00000590329.5 | hg19 | chr19 | 11,033,948 | 11,039,261 | 5,314 |
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