INS-IGF2 INS-IGF2 readthrough

Information
Symbol
INS-IGF2
Type
protein-coding
Description
INS-IGF2 readthrough
Entrez Gene ID
723961
Genome
hg19
Position
chr11:2,167,856-2,182,439
Genome
hg38
Position
chr11:2,146,626-2,161,209
HGNC
HGNC:33527 HGNC
Ensembl
ENSG00000129965 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 14 18
Likely pathogenic 0 34
Benign 0 38
Likely benign 0 58
Conflicting classifications of pathogenicity 0 52
Likely risk allele 0 22
not provided 2 10
Uncertain risk allele 0 4
Uncertain significance 0 94
Ranking
ClinVar
0
0
48
174
10
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 INSIGF
HGNC HGNC:33527 HGNC
Ensembl ENSG00000129965 Ensembl
AllianceGenome HGNC:33527
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000397270.1 hg38 chr11 2,146,626 2,161,209 14,584
ENST00000397270.1 hg19 chr11 2,167,856 2,182,439 14,584
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