IFT70B intraflagellar transport 70B

Information
Symbol
IFT70B
Type
protein-coding
Description
intraflagellar transport 70B
Entrez Gene ID
150737
Genome
hg19
Position
chr2:178,413,726-178,417,524
Genome
hg38
Position
chr2:177,548,998-177,552,796
MIM
620742 OMIM
HGNC
HGNC:26425 HGNC
Ensembl
ENSG00000196659 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 14
Uncertain significance 0 76
Ranking
ClinVar
0
0
2
92
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 :
Filtering :
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 IFT70
SYNONYM TTC30B
SYNONYM fleer
MIM 620742 OMIM
HGNC HGNC:26425 HGNC
Ensembl ENSG00000196659 Ensembl
AllianceGenome HGNC:26425
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000408939.4 hg38 chr2 177,548,998 177,552,796 3,799
ENST00000408939.4 hg19 chr2 178,413,726 178,417,524 3,799
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