CYP2F1 cytochrome P450 family 2 subfamily F member 1
Information
- Symbol
- CYP2F1
- Type
- protein-coding
- Description
- cytochrome P450 family 2 subfamily F member 1
- Entrez Gene ID
- 1572
- Genome
- hg19
- Position
- chr19:41,620,337-41,634,286
- Genome
- hg38
- Position
- chr19:41,114,432-41,128,381
- MIM
- 124070 OMIM
- HGNC
- HGNC:2632 HGNC
- Ensembl
- ENSG00000197446 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 16 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 72 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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90 |
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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 |
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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 |
---|---|
SYNONYM | C2F1 |
SYNONYM | CYP2F |
SYNONYM | CYPIIF1 |
MIM | 124070 OMIM |
HGNC | HGNC:2632 HGNC |
Ensembl | ENSG00000197446 Ensembl |
AllianceGenome | HGNC:2632 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000331105.7 | hg38 | chr19 | 41,114,432 | 41,128,381 | 13,950 |
ENST00000331105.7 | hg19 | chr19 | 41,620,337 | 41,634,286 | 13,950 |
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