ARHGEF38 Rho guanine nucleotide exchange factor 38
Information
- Symbol
- ARHGEF38
- Type
- protein-coding
- Description
- Rho guanine nucleotide exchange factor 38
- Entrez Gene ID
- 54848
- Genome
- hg19
- Position
- chr4:106,473,777-106,602,071
- Genome
- hg38
- Position
- chr4:105,552,620-105,680,914
- MIM
- 619919 OMIM
- HGNC
- HGNC:25968 HGNC
- Ensembl
- ENSG00000236699 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 78 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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80 |
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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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Category | : |
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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 |
---|---|
MIM | 619919 OMIM |
HGNC | HGNC:25968 HGNC |
Ensembl | ENSG00000236699 Ensembl |
AllianceGenome | HGNC:25968 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000420470.3 | hg38 | chr4 | 105,552,620 | 105,680,914 | 128,295 |
ENST00000265154.6 | hg38 | chr4 | 105,552,620 | 105,631,680 | 79,061 |
ENST00000265154.6 | hg19 | chr4 | 106,473,777 | 106,552,837 | 79,061 |
ENST00000420470.3 | hg19 | chr4 | 106,473,777 | 106,602,071 | 128,295 |
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