MAFTRR MAF transcriptional regulator RNA
Information
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 |
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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Filtering | : |
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 | linc-MAF-4 |
SYNONYM | lincMAF4 |
MIM | 616264 OMIM |
HGNC | HGNC:51525 HGNC |
Ensembl | ENSG00000261390 Ensembl |
AllianceGenome | HGNC:51525 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000658463.1 | hg38 | chr16 | 79,715,231 | 79,770,561 | 55,331 |
ENST00000567993.8 | hg38 | chr16 | 79,721,304 | 79,770,569 | 49,266 |
ENST00000668946.1 | hg38 | chr16 | 79,715,224 | 79,770,570 | 55,347 |
ENST00000562921.6 | hg38 | chr16 | 79,715,220 | 79,770,566 | 55,347 |
ENST00000685222.1 | hg38 | chr16 | 79,721,308 | 79,770,333 | 49,026 |
ENST00000662553.1 | hg38 | chr16 | 79,750,115 | 79,770,567 | 20,453 |
ENST00000562921.6 | hg19 | chr16 | 79,749,117 | 79,804,463 | 55,347 |
ENST00000668946.1 | hg19 | chr16 | 79,749,121 | 79,804,467 | 55,347 |
ENST00000658463.1 | hg19 | chr16 | 79,749,128 | 79,804,458 | 55,331 |
ENST00000567993.8 | hg19 | chr16 | 79,755,201 | 79,804,466 | 49,266 |
ENST00000662553.1 | hg19 | chr16 | 79,784,012 | 79,804,464 | 20,453 |
ENST00000685222.1 | hg19 | chr16 | 79,755,205 | 79,804,230 | 49,026 |
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