AIF1 allograft inflammatory factor 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 1 | 0 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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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
Locus Zoom
Variants
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
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MGeND data only
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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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SYNONYM | AIF-1 |
SYNONYM | IBA1 |
SYNONYM | IRT-1 |
SYNONYM | IRT1 |
MIM | 601833 OMIM |
HGNC | HGNC:352 HGNC |
Ensembl | ENSG00000204472 Ensembl |
AllianceGenome | HGNC:352 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000376059.8 | hg38 | chr6 | 31,615,234 | 31,617,015 | 1,782 |
ENST00000376049.4 | hg38 | chr6 | 31,615,991 | 31,617,021 | 1,031 |
ENST00000376059.8 | hg19 | chr6 | 31,583,011 | 31,584,792 | 1,782 |
ENST00000376049.4 | hg19 | chr6 | 31,583,768 | 31,584,798 | 1,031 |
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