NAIF1 nuclear apoptosis inducing factor 1
Information
- Symbol
- NAIF1
- Type
- protein-coding
- Description
- nuclear apoptosis inducing factor 1
- Entrez Gene ID
- 203245
- Genome
- hg19
- Position
- chr9:130,823,512-130,829,599
- Genome
- hg38
- Position
- chr9:128,061,233-128,067,320
- MIM
- 610673 OMIM
- HGNC
- HGNC:25446 HGNC
- Ensembl
- ENSG00000171169 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 1 | 0 |
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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24 |
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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
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 |
---|---|
SYNONYM | C9orf90 |
SYNONYM | bA379C10.2 |
MIM | 610673 OMIM |
HGNC | HGNC:25446 HGNC |
Ensembl | ENSG00000171169 Ensembl |
AllianceGenome | HGNC:25446 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000373078.5 | hg38 | chr9 | 128,061,233 | 128,067,320 | 6,088 |
ENST00000373078.5 | hg19 | chr9 | 130,823,512 | 130,829,599 | 6,088 |
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