GTF2F2 general transcription factor IIF subunit 2
Information
- Symbol
- GTF2F2
- Type
- protein-coding
- Description
- general transcription factor IIF subunit 2
- Entrez Gene ID
- 2963
- Genome
- hg19
- Position
- chr13:45,694,645-45,859,028
- Genome
- hg38
- Position
- chr13:45,120,510-45,284,893
- MIM
- 189969 OMIM
- HGNC
- HGNC:4653 HGNC
- Ensembl
- ENSG00000188342 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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44 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
Type | ID |
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SYNONYM | BTF4 |
SYNONYM | RAP30 |
SYNONYM | TF2F2 |
SYNONYM | TFIIF |
MIM | 189969 OMIM |
HGNC | HGNC:4653 HGNC |
Ensembl | ENSG00000188342 Ensembl |
AllianceGenome | HGNC:4653 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000340473.8 | hg38 | chr13 | 45,120,510 | 45,284,893 | 164,384 |
ENST00000340473.8 | hg19 | chr13 | 45,694,645 | 45,859,028 | 164,384 |
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