PLD2 phospholipase D2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 12 |
Uncertain significance | 0 | 126 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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148 |
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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
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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 |
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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 | PLD1C |
MIM | 602384 OMIM |
HGNC | HGNC:9068 HGNC |
Ensembl | ENSG00000129219 Ensembl |
AllianceGenome | HGNC:9068 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000572940.5 | hg38 | chr17 | 4,807,169 | 4,823,428 | 16,260 |
ENST00000263088.11 | hg38 | chr17 | 4,807,152 | 4,823,430 | 16,279 |
ENST00000263088.11 | hg19 | chr17 | 4,710,447 | 4,726,725 | 16,279 |
ENST00000572940.5 | hg19 | chr17 | 4,710,464 | 4,726,723 | 16,260 |
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