NUCB1 nucleobindin 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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64 |
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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
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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 | CALNUC |
SYNONYM | NUC |
MIM | 601323 OMIM |
HGNC | HGNC:8043 HGNC |
Ensembl | ENSG00000104805 Ensembl |
AllianceGenome | HGNC:8043 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000407032.5 | hg38 | chr19 | 48,900,320 | 48,923,271 | 22,952 |
ENST00000452087.6 | hg38 | chr19 | 48,900,279 | 48,923,255 | 22,977 |
ENST00000424608.2 | hg38 | chr19 | 48,900,050 | 48,923,271 | 23,222 |
ENST00000706759.1 | hg38 | chr19 | 48,900,281 | 48,923,255 | 22,975 |
ENST00000706757.1 | hg38 | chr19 | 48,900,279 | 48,923,255 | 22,977 |
ENST00000706753.1 | hg38 | chr19 | 48,900,279 | 48,923,255 | 22,977 |
ENST00000706760.1 | hg38 | chr19 | 48,900,303 | 48,923,255 | 22,953 |
ENST00000706749.1 | hg38 | chr19 | 48,900,279 | 48,923,079 | 22,801 |
ENST00000706748.1 | hg38 | chr19 | 48,900,279 | 48,923,012 | 22,734 |
ENST00000706746.1 | hg38 | chr19 | 48,900,279 | 48,922,988 | 22,710 |
ENST00000451312.6 | hg38 | chr19 | 48,900,566 | 48,923,272 | 22,707 |
ENST00000405315.9 | hg38 | chr19 | 48,900,312 | 48,923,372 | 23,061 |
ENST00000424608.2 | hg19 | chr19 | 49,403,307 | 49,426,528 | 23,222 |
ENST00000405315.9 | hg19 | chr19 | 49,403,569 | 49,426,629 | 23,061 |
ENST00000407032.5 | hg19 | chr19 | 49,403,577 | 49,426,528 | 22,952 |
ENST00000451312.6 | hg19 | chr19 | 49,403,823 | 49,426,529 | 22,707 |
ENST00000706746.1 | hg19 | chr19 | 49,403,536 | 49,426,245 | 22,710 |
ENST00000706748.1 | hg19 | chr19 | 49,403,536 | 49,426,269 | 22,734 |
ENST00000706749.1 | hg19 | chr19 | 49,403,536 | 49,426,336 | 22,801 |
ENST00000452087.6 | hg19 | chr19 | 49,403,536 | 49,426,512 | 22,977 |
ENST00000706753.1 | hg19 | chr19 | 49,403,536 | 49,426,512 | 22,977 |
ENST00000706757.1 | hg19 | chr19 | 49,403,536 | 49,426,512 | 22,977 |
ENST00000706759.1 | hg19 | chr19 | 49,403,538 | 49,426,512 | 22,975 |
ENST00000706760.1 | hg19 | chr19 | 49,403,560 | 49,426,512 | 22,953 |
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