NXF1 nuclear RNA export factor 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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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 |
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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 | MEX67 |
SYNONYM | TAP |
MIM | 602647 OMIM |
HGNC | HGNC:8071 HGNC |
Ensembl | ENSG00000162231 Ensembl |
AllianceGenome | HGNC:8071 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000531709.6 | hg38 | chr11 | 62,792,123 | 62,805,470 | 13,348 |
ENST00000531131.1 | hg38 | chr11 | 62,800,113 | 62,805,440 | 5,328 |
ENST00000532297.5 | hg38 | chr11 | 62,792,171 | 62,806,302 | 14,132 |
ENST00000294172.7 | hg38 | chr11 | 62,792,130 | 62,805,440 | 13,311 |
ENST00000294172.7 | hg19 | chr11 | 62,559,602 | 62,572,912 | 13,311 |
ENST00000531709.6 | hg19 | chr11 | 62,559,595 | 62,572,942 | 13,348 |
ENST00000531131.1 | hg19 | chr11 | 62,567,585 | 62,572,912 | 5,328 |
ENST00000532297.5 | hg19 | chr11 | 62,559,643 | 62,573,774 | 14,132 |
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