MFF-DT MFF divergent transcript
Information
- Symbol
- MFF-DT
- Type
- ncRNA
- Description
- MFF divergent transcript
- Entrez Gene ID
- 654841
- Genome
- hg19
- Position
- chr2:228,101,410-228,189,904
- Genome
- hg38
- Position
- chr2:227,236,694-227,325,188
- HGNC
- HGNC:41067 HGNC
- Ensembl
- ENSG00000236432 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 2 | 0 |
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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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
|
Category | : |
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Search word | : | |
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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000671563.1 | hg38 | chr2 | 227,245,723 | 227,325,474 | 79,752 |
ENST00000666788.1 | hg38 | chr2 | 227,245,722 | 227,285,261 | 39,540 |
ENST00000433324.2 | hg38 | chr2 | 227,236,694 | 227,325,188 | 88,495 |
ENST00000439598.6 | hg38 | chr2 | 227,221,052 | 227,325,164 | 104,113 |
ENST00000670070.1 | hg38 | chr2 | 227,235,441 | 227,325,226 | 89,786 |
ENST00000396588.6 | hg38 | chr2 | 227,245,710 | 227,325,186 | 79,477 |
ENST00000665988.1 | hg38 | chr2 | 227,235,809 | 227,325,711 | 89,903 |
ENST00000433324.2 | hg19 | chr2 | 228,101,410 | 228,189,904 | 88,495 |
ENST00000439598.6 | hg19 | chr2 | 228,085,768 | 228,189,880 | 104,113 |
ENST00000396588.6 | hg19 | chr2 | 228,110,426 | 228,189,902 | 79,477 |
ENST00000665988.1 | hg19 | chr2 | 228,100,525 | 228,190,427 | 89,903 |
ENST00000666788.1 | hg19 | chr2 | 228,110,438 | 228,149,977 | 39,540 |
ENST00000671563.1 | hg19 | chr2 | 228,110,439 | 228,190,190 | 79,752 |
ENST00000670070.1 | hg19 | chr2 | 228,100,157 | 228,189,942 | 89,786 |
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