CYP3A43 cytochrome P450 family 3 subfamily A member 43
Information
- Symbol
- CYP3A43
- Type
- protein-coding
- Description
- cytochrome P450 family 3 subfamily A member 43
- Entrez Gene ID
- 64816
- Genome
- hg19
- Position
- chr7:99,425,739-99,463,624
- Genome
- hg38
- Position
- chr7:99,828,116-99,866,001
- MIM
- 606534 OMIM
- HGNC
- HGNC:17450 HGNC
- Ensembl
- ENSG00000021461 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 38 |
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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
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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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Category | : |
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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 |
---|---|
MIM | 606534 OMIM |
HGNC | HGNC:17450 HGNC |
Ensembl | ENSG00000021461 Ensembl |
AllianceGenome | HGNC:17450 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000354829.7 | hg38 | chr7 | 99,828,013 | 99,866,093 | 38,081 |
ENST00000444905.5 | hg38 | chr7 | 99,828,049 | 99,866,045 | 37,997 |
ENST00000312017.9 | hg38 | chr7 | 99,828,116 | 99,866,001 | 37,886 |
ENST00000415413.5 | hg38 | chr7 | 99,828,049 | 99,866,045 | 37,997 |
ENST00000417625.5 | hg38 | chr7 | 99,828,043 | 99,866,001 | 37,959 |
ENST00000222382.5 | hg38 | chr7 | 99,828,116 | 99,866,001 | 37,886 |
ENST00000631161.2 | hg38 | chr7 | 99,828,013 | 99,839,420 | 11,408 |
ENST00000631161.2 | hg19 | chr7 | 99,425,636 | 99,437,043 | 11,408 |
ENST00000354829.7 | hg19 | chr7 | 99,425,636 | 99,463,716 | 38,081 |
ENST00000417625.5 | hg19 | chr7 | 99,425,666 | 99,463,624 | 37,959 |
ENST00000415413.5 | hg19 | chr7 | 99,425,672 | 99,463,668 | 37,997 |
ENST00000444905.5 | hg19 | chr7 | 99,425,672 | 99,463,668 | 37,997 |
ENST00000222382.5 | hg19 | chr7 | 99,425,739 | 99,463,624 | 37,886 |
ENST00000312017.9 | hg19 | chr7 | 99,425,739 | 99,463,624 | 37,886 |
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