ABCF3 ATP binding cassette subfamily F member 3
Information
- Symbol
- ABCF3
- Type
- protein-coding
- Description
- ATP binding cassette subfamily F member 3
- Entrez Gene ID
- 55324
- Genome
- hg19
- Position
- chr3:183,903,987-183,911,793
- Genome
- hg38
- Position
- chr3:184,186,199-184,194,005
- MIM
- 618967 OMIM
- HGNC
- HGNC:72 HGNC
- Ensembl
- ENSG00000161204 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 1 | 0 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 68 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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68 |
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2 |
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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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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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
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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 |
Type | ID |
---|---|
SYNONYM | EST201864 |
MIM | 618967 OMIM |
HGNC | HGNC:72 HGNC |
Ensembl | ENSG00000161204 Ensembl |
AllianceGenome | HGNC:72 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000292808.5 | hg38 | chr3 | 184,186,174 | 184,194,005 | 7,832 |
ENST00000429586.7 | hg38 | chr3 | 184,186,199 | 184,194,005 | 7,807 |
ENST00000292808.5 | hg19 | chr3 | 183,903,962 | 183,911,793 | 7,832 |
ENST00000429586.7 | hg19 | chr3 | 183,903,987 | 183,911,793 | 7,807 |
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