CYP20A1 cytochrome P450 family 20 subfamily A member 1
Information
- Symbol
- CYP20A1
- Type
- protein-coding
- Description
- cytochrome P450 family 20 subfamily A member 1
- Entrez Gene ID
- 57404
- Genome
- hg19
- Position
- chr2:204,103,705-204,161,949
- Genome
- hg38
- Position
- chr2:203,238,982-203,297,226
- HGNC
- HGNC:20576 HGNC
- Ensembl
- ENSG00000119004 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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52 |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000429815.6 | hg38 | chr2 | 203,238,982 | 203,297,226 | 58,245 |
ENST00000356079.9 | hg38 | chr2 | 203,239,018 | 203,306,026 | 67,009 |
ENST00000429815.6 | hg19 | chr2 | 204,103,705 | 204,161,949 | 58,245 |
ENST00000356079.9 | hg19 | chr2 | 204,103,741 | 204,170,749 | 67,009 |
Key | Value |
---|---|
strand | + |
start | 204,103,163 |
Gene Symbol | CYP20A1 |
Entrez GeneId | 57,404 |
Chr Band | 2q33.2 |
end | 204,170,562 |
chr | chr2 |
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