PLA2G2A phospholipase A2 group IIA
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 10 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 12 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
2 |
 |
26 |
 |
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
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | MOM1 |
| SYNONYM | PLA2 |
| SYNONYM | PLA2B |
| SYNONYM | PLA2L |
| SYNONYM | PLA2S |
| SYNONYM | PLAS1 |
| SYNONYM | sPLA2 |
| MIM | 172411 OMIM |
| HGNC | HGNC:9031 HGNC |
| Ensembl | ENSG00000188257 Ensembl |
| AllianceGenome | HGNC:9031 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000400520.8 | hg38 | chr1 | 19,975,431 | 19,979,607 | 4,177 |
| ENST00000482011.3 | hg38 | chr1 | 19,975,435 | 19,979,618 | 4,184 |
| ENST00000649436.1 | hg38 | chr1 | 19,975,431 | 19,979,621 | 4,191 |
| ENST00000375111.7 | hg38 | chr1 | 19,975,438 | 19,980,416 | 4,979 |
| ENST00000400520.8 | hg19 | chr1 | 20,301,924 | 20,306,100 | 4,177 |
| ENST00000649436.1 | hg19 | chr1 | 20,301,924 | 20,306,114 | 4,191 |
| ENST00000482011.3 | hg19 | chr1 | 20,301,928 | 20,306,111 | 4,184 |
| ENST00000375111.7 | hg19 | chr1 | 20,301,931 | 20,306,909 | 4,979 |
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