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
0
0
0
174
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
Category :
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CDEP
SYNONYM FARP1-IT1
SYNONYM GLCC1
SYNONYM PLEKHC2
SYNONYM PPP1R75
MIM 602654 OMIM
HGNC HGNC:3591 HGNC
Ensembl ENSG00000152767 Ensembl
AllianceGenome HGNC:3591
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
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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