FIGNL1 fidgetin like 1

Information
Symbol
FIGNL1
Type
protein-coding
Description
fidgetin like 1
Entrez Gene ID
63979
Genome
hg19
Position
chr7:50,511,831-50,518,048
Genome
hg38
Position
chr7:50,444,133-50,450,350
MIM
615383 OMIM
HGNC
HGNC:13286 HGNC
Ensembl
ENSG00000132436 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
Uncertain significance 0 82
Ranking
ClinVar
0
0
0
90
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 :
Search word :
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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
MIM 615383 OMIM
HGNC HGNC:13286 HGNC
Ensembl ENSG00000132436 Ensembl
AllianceGenome HGNC:13286
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000395556.6 hg38 chr7 50,444,133 50,450,350 6,218
ENST00000356889.8 hg38 chr7 50,444,128 50,450,324 6,197
ENST00000435566.5 hg38 chr7 50,446,787 50,450,388 3,602
ENST00000419119.1 hg38 chr7 50,445,142 50,449,724 4,583
ENST00000615084.4 hg38 chr7 50,444,129 50,450,390 6,262
ENST00000617389.4 hg38 chr7 50,444,129 50,450,390 6,262
ENST00000433017.6 hg38 chr7 50,444,133 50,450,350 6,218
ENST00000356889.8 hg19 chr7 50,511,826 50,518,022 6,197
ENST00000615084.4 hg19 chr7 50,511,827 50,518,088 6,262
ENST00000617389.4 hg19 chr7 50,511,827 50,518,088 6,262
ENST00000395556.6 hg19 chr7 50,511,831 50,518,048 6,218
ENST00000433017.6 hg19 chr7 50,511,831 50,518,048 6,218
ENST00000419119.1 hg19 chr7 50,512,840 50,517,422 4,583
ENST00000435566.5 hg19 chr7 50,514,485 50,518,086 3,602
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