GNLY granulysin
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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20 |
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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 | D2S69E |
SYNONYM | LAG-2 |
SYNONYM | LAG2 |
SYNONYM | NKG5 |
SYNONYM | TLA519 |
MIM | 188855 OMIM |
HGNC | HGNC:4414 HGNC |
Ensembl | ENSG00000115523 Ensembl |
AllianceGenome | HGNC:4414 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409696.7 | hg38 | chr2 | 85,694,426 | 85,698,757 | 4,332 |
ENST00000524600.5 | hg38 | chr2 | 85,694,358 | 85,698,744 | 4,387 |
ENST00000263863.9 | hg38 | chr2 | 85,694,358 | 85,698,852 | 4,495 |
ENST00000524600.5 | hg19 | chr2 | 85,921,481 | 85,925,867 | 4,387 |
ENST00000263863.9 | hg19 | chr2 | 85,921,481 | 85,925,975 | 4,495 |
ENST00000409696.7 | hg19 | chr2 | 85,921,549 | 85,925,880 | 4,332 |
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