NGFR nerve growth factor receptor
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 14 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 50 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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70 |
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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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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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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 | CD271 |
SYNONYM | Gp80-LNGFR |
SYNONYM | TNFRSF16 |
SYNONYM | p75(NTR) |
SYNONYM | p75NTR |
MIM | 162010 OMIM |
HGNC | HGNC:7809 HGNC |
Ensembl | ENSG00000064300 Ensembl |
AllianceGenome | HGNC:7809 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000504201.1 | hg38 | chr17 | 49,497,391 | 49,513,372 | 15,982 |
ENST00000172229.8 | hg38 | chr17 | 49,495,293 | 49,515,008 | 19,716 |
ENST00000172229.8 | hg19 | chr17 | 47,572,655 | 47,592,370 | 19,716 |
ENST00000504201.1 | hg19 | chr17 | 47,574,753 | 47,590,734 | 15,982 |
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