FAIM2 Fas apoptotic inhibitory molecule 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
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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20 |
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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 |
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Target data | : |
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 | LFG |
SYNONYM | LFG2 |
SYNONYM | NGP35 |
SYNONYM | NMP35 |
SYNONYM | TMBIM2 |
MIM | 604306 OMIM |
HGNC | HGNC:17067 HGNC |
Ensembl | ENSG00000135472 Ensembl |
AllianceGenome | HGNC:17067 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000320634.8 | hg38 | chr12 | 49,866,896 | 49,903,900 | 37,005 |
ENST00000550890.5 | hg38 | chr12 | 49,870,400 | 49,902,379 | 31,980 |
ENST00000320634.8 | hg19 | chr12 | 50,260,679 | 50,297,683 | 37,005 |
ENST00000550890.5 | hg19 | chr12 | 50,264,183 | 50,296,162 | 31,980 |
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