IGFL4 IGF like family member 4
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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MIM | 610547 OMIM |
HGNC | HGNC:32931 HGNC |
Ensembl | ENSG00000204869 Ensembl |
AllianceGenome | HGNC:32931 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000377697.2 | hg38 | chr19 | 46,039,182 | 46,041,002 | 1,821 |
ENST00000601672.5 | hg38 | chr19 | 46,039,824 | 46,077,094 | 37,271 |
ENST00000377697.2 | hg19 | chr19 | 46,542,440 | 46,544,260 | 1,821 |
ENST00000601672.5 | hg19 | chr19 | 46,543,082 | 46,580,352 | 37,271 |
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