RFX2 regulatory factor X2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 12 |
Uncertain significance | 0 | 94 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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108 |
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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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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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ENST00000592546.5 | hg38 | chr19 | 5,994,502 | 6,110,532 | 116,031 |
ENST00000303657.10 | hg38 | chr19 | 5,993,164 | 6,110,500 | 117,337 |
ENST00000359161.7 | hg38 | chr19 | 5,993,517 | 6,049,232 | 55,716 |
ENST00000303657.10 | hg19 | chr19 | 5,993,175 | 6,110,511 | 117,337 |
ENST00000359161.7 | hg19 | chr19 | 5,993,528 | 6,049,243 | 55,716 |
ENST00000592546.5 | hg19 | chr19 | 5,994,513 | 6,110,543 | 116,031 |
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