FARP1 FERM, ARH/RhoGEF and pleckstrin domain protein 1
Information
- Symbol
- FARP1
- Type
- protein-coding
- Description
- FERM, ARH/RhoGEF and pleckstrin domain protein 1
- Entrez Gene ID
- 10160
- Genome
- hg19
- Position
- chr13:98,794,816-99,102,027
- Genome
- hg38
- Position
- chr13:98,142,562-98,449,773
- MIM
- 602654 OMIM
- HGNC
- HGNC:3591 HGNC
- Ensembl
- ENSG00000152767 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 164 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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174 |
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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
Target data | : |
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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Search word | : | |
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 |
---|---|
SYNONYM | CDEP |
SYNONYM | FARP1-IT1 |
SYNONYM | GLCC1 |
SYNONYM | PLEKHC2 |
SYNONYM | PPP1R75 |
MIM | 602654 OMIM |
HGNC | HGNC:3591 HGNC |
Ensembl | ENSG00000152767 Ensembl |
AllianceGenome | HGNC:3591 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000595437.5 | hg38 | chr13 | 98,142,562 | 98,449,773 | 307,212 |
ENST00000596580.2 | hg38 | chr13 | 98,143,416 | 98,407,494 | 264,079 |
ENST00000376581.9 | hg38 | chr13 | 98,143,480 | 98,245,304 | 101,825 |
ENST00000627049.2 | hg38 | chr13 | 98,143,098 | 98,449,771 | 306,674 |
ENST00000319562.11 | hg38 | chr13 | 98,143,094 | 98,455,176 | 312,083 |
ENST00000319562.11 | hg19 | chr13 | 98,795,348 | 99,107,430 | 312,083 |
ENST00000376581.9 | hg19 | chr13 | 98,795,734 | 98,897,558 | 101,825 |
ENST00000595437.5 | hg19 | chr13 | 98,794,816 | 99,102,027 | 307,212 |
ENST00000596580.2 | hg19 | chr13 | 98,795,670 | 99,059,748 | 264,079 |
ENST00000627049.2 | hg19 | chr13 | 98,795,352 | 99,102,025 | 306,674 |
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