FHOD1 formin homology 2 domain containing 1

Information
Symbol
FHOD1
Type
protein-coding
Description
formin homology 2 domain containing 1
Entrez Gene ID
29109
Genome
hg19
Position
chr16:67,263,292-67,281,384
Genome
hg38
Position
chr16:67,229,389-67,247,481
MIM
606881 OMIM
HGNC
HGNC:17905 HGNC
Ensembl
ENSG00000135723 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 0 2
Uncertain significance 0 158
Ranking
ClinVar
0
0
0
164
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 FHOS
MIM 606881 OMIM
HGNC HGNC:17905 HGNC
Ensembl ENSG00000135723 Ensembl
AllianceGenome HGNC:17905
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000258201.9 hg38 chr16 67,229,389 67,247,481 18,093
ENST00000258201.9 hg19 chr16 67,263,292 67,281,384 18,093
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