NLRX1 NLR family member X1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 8 |
not provided | 0 | 46 |
Uncertain significance | 0 | 134 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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146 |
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2 |
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 |
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 | |||
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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 |
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SYNONYM | CLR11.3 |
SYNONYM | DLNB26 |
SYNONYM | NOD26 |
SYNONYM | NOD5 |
SYNONYM | NOD9 |
MIM | 611947 OMIM |
HGNC | HGNC:29890 HGNC |
Ensembl | ENSG00000160703 Ensembl |
AllianceGenome | HGNC:29890 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000474751.7 | hg38 | chr11 | 119,168,748 | 119,183,985 | 15,238 |
ENST00000706729.1 | hg38 | chr11 | 119,168,754 | 119,183,985 | 15,232 |
ENST00000706727.1 | hg38 | chr11 | 119,168,747 | 119,183,991 | 15,245 |
ENST00000706728.1 | hg38 | chr11 | 119,168,748 | 119,183,950 | 15,203 |
ENST00000525863.1 | hg38 | chr11 | 119,171,356 | 119,184,016 | 12,661 |
ENST00000292199.6 | hg38 | chr11 | 119,168,729 | 119,184,014 | 15,286 |
ENST00000409109.6 | hg38 | chr11 | 119,168,725 | 119,184,016 | 15,292 |
ENST00000409991.5 | hg38 | chr11 | 119,168,728 | 119,184,012 | 15,285 |
ENST00000409109.6 | hg19 | chr11 | 119,039,434 | 119,054,725 | 15,292 |
ENST00000409991.5 | hg19 | chr11 | 119,039,437 | 119,054,721 | 15,285 |
ENST00000292199.6 | hg19 | chr11 | 119,039,438 | 119,054,723 | 15,286 |
ENST00000706727.1 | hg19 | chr11 | 119,039,456 | 119,054,700 | 15,245 |
ENST00000706728.1 | hg19 | chr11 | 119,039,457 | 119,054,659 | 15,203 |
ENST00000474751.7 | hg19 | chr11 | 119,039,457 | 119,054,694 | 15,238 |
ENST00000706729.1 | hg19 | chr11 | 119,039,463 | 119,054,694 | 15,232 |
ENST00000525863.1 | hg19 | chr11 | 119,042,065 | 119,054,725 | 12,661 |
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