NRSN1 neurensin 1
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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26 |
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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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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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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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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 | VMP |
SYNONYM | p24 |
MIM | 616630 OMIM |
HGNC | HGNC:17881 HGNC |
Ensembl | ENSG00000152954 Ensembl |
AllianceGenome | HGNC:17881 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000378475.1 | hg38 | chr6 | 24,134,317 | 24,141,523 | 7,207 |
ENST00000378478.5 | hg38 | chr6 | 24,126,186 | 24,147,529 | 21,344 |
ENST00000378491.9 | hg38 | chr6 | 24,126,215 | 24,147,530 | 21,316 |
ENST00000378478.5 | hg19 | chr6 | 24,126,414 | 24,147,757 | 21,344 |
ENST00000378491.9 | hg19 | chr6 | 24,126,443 | 24,147,758 | 21,316 |
ENST00000378475.1 | hg19 | chr6 | 24,134,545 | 24,141,751 | 7,207 |
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