NKG7 natural killer cell granule protein 7
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
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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36 |
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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 |
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SYNONYM | GIG1 |
SYNONYM | GMP-17 |
SYNONYM | p15-TIA-1 |
MIM | 606008 OMIM |
HGNC | HGNC:7830 HGNC |
Ensembl | ENSG00000105374 Ensembl |
AllianceGenome | HGNC:7830 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000600427.5 | hg38 | chr19 | 51,371,620 | 51,372,640 | 1,021 |
ENST00000221978.10 | hg38 | chr19 | 51,371,620 | 51,372,654 | 1,035 |
ENST00000595217.1 | hg38 | chr19 | 51,371,606 | 51,372,701 | 1,096 |
ENST00000595217.1 | hg19 | chr19 | 51,874,860 | 51,875,955 | 1,096 |
ENST00000600427.5 | hg19 | chr19 | 51,874,874 | 51,875,894 | 1,021 |
ENST00000221978.10 | hg19 | chr19 | 51,874,874 | 51,875,908 | 1,035 |
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