NFKBID NFKB inhibitor delta
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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4 |
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 | IkBNS |
SYNONYM | IkappaBNS |
SYNONYM | TA-NFKBH |
MIM | 618887 OMIM |
HGNC | HGNC:15671 HGNC |
Ensembl | ENSG00000167604 Ensembl |
AllianceGenome | HGNC:15671 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000585544.2 | hg38 | chr19 | 35,887,956 | 35,899,740 | 11,785 |
ENST00000585925.8 | hg38 | chr19 | 35,887,630 | 35,900,662 | 13,033 |
ENST00000715565.1 | hg38 | chr19 | 35,887,680 | 35,899,737 | 12,058 |
ENST00000606253.5 | hg38 | chr19 | 35,888,241 | 35,902,303 | 14,063 |
ENST00000641389.3 | hg38 | chr19 | 35,887,952 | 35,900,540 | 12,589 |
ENST00000585925.8 | hg19 | chr19 | 36,378,532 | 36,391,564 | 13,033 |
ENST00000715565.1 | hg19 | chr19 | 36,378,582 | 36,390,639 | 12,058 |
ENST00000641389.3 | hg19 | chr19 | 36,378,854 | 36,391,442 | 12,589 |
ENST00000585544.2 | hg19 | chr19 | 36,378,858 | 36,390,642 | 11,785 |
ENST00000606253.5 | hg19 | chr19 | 36,379,143 | 36,393,205 | 14,063 |
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