NKIRAS1 NFKB inhibitor interacting Ras like 1
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 16 |
| Likely pathogenic | 0 | 2 |
| Benign | 0 | 38 |
| Likely benign | 0 | 100 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 130 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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32 |
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244 |
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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
[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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | KBRAS1 |
| SYNONYM | kappaB-Ras1 |
| MIM | 604496 OMIM |
| HGNC | HGNC:17899 HGNC |
| Ensembl | ENSG00000197885 Ensembl |
| AllianceGenome | HGNC:17899 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000412028.5 | hg38 | chr3 | 23,892,307 | 23,916,963 | 24,657 |
| ENST00000416026.2 | hg38 | chr3 | 23,893,065 | 23,916,952 | 23,888 |
| ENST00000425478.7 | hg38 | chr3 | 23,889,951 | 23,916,990 | 27,040 |
| ENST00000388759.7 | hg38 | chr3 | 23,891,660 | 23,916,969 | 25,310 |
| ENST00000421515.6 | hg38 | chr3 | 23,892,064 | 23,946,591 | 54,528 |
| ENST00000415901.6 | hg38 | chr3 | 23,892,310 | 23,916,924 | 24,615 |
| ENST00000614374.4 | hg38 | chr3 | 23,892,083 | 23,910,925 | 18,843 |
| ENST00000443659.6 | hg38 | chr3 | 23,892,061 | 23,916,715 | 24,655 |
| ENST00000437230.5 | hg38 | chr3 | 23,892,097 | 23,916,969 | 24,873 |
| ENST00000425478.7 | hg19 | chr3 | 23,931,442 | 23,958,481 | 27,040 |
| ENST00000388759.7 | hg19 | chr3 | 23,933,151 | 23,958,460 | 25,310 |
| ENST00000443659.6 | hg19 | chr3 | 23,933,552 | 23,958,206 | 24,655 |
| ENST00000421515.6 | hg19 | chr3 | 23,933,555 | 23,988,082 | 54,528 |
| ENST00000614374.4 | hg19 | chr3 | 23,933,574 | 23,952,416 | 18,843 |
| ENST00000437230.5 | hg19 | chr3 | 23,933,588 | 23,958,460 | 24,873 |
| ENST00000412028.5 | hg19 | chr3 | 23,933,798 | 23,958,454 | 24,657 |
| ENST00000415901.6 | hg19 | chr3 | 23,933,801 | 23,958,415 | 24,615 |
| ENST00000416026.2 | hg19 | chr3 | 23,934,556 | 23,958,443 | 23,888 |
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