ARHGEF35 Rho guanine nucleotide exchange factor 35
Information
- Symbol
- ARHGEF35
- Type
- protein-coding
- Description
- Rho guanine nucleotide exchange factor 35
- Entrez Gene ID
- 445328
- Genome
- hg19
- Position
- chr7:143,883,176-143,892,926
- Genome
- hg38
- Position
- chr7:144,186,083-144,195,833
- HGNC
- HGNC:33846 HGNC
- Ensembl
- ENSG00000213214 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 14 |
Uncertain significance | 0 | 54 |
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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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 | ARHGEF5L |
HGNC | HGNC:33846 HGNC |
Ensembl | ENSG00000213214 Ensembl |
AllianceGenome | HGNC:33846 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000688754.1 | hg38 | chr7 | 144,186,083 | 144,195,879 | 9,797 |
ENST00000378115.3 | hg38 | chr7 | 144,186,083 | 144,195,833 | 9,751 |
ENST00000378115.3 | hg19 | chr7 | 143,883,176 | 143,892,926 | 9,751 |
ENST00000688754.1 | hg19 | chr7 | 143,883,176 | 143,892,972 | 9,797 |
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