IL19 interleukin 19
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 2 |
| Benign | 0 | 14 |
| Likely benign | 0 | 80 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| not provided | 2 | 0 |
| Uncertain risk allele | 0 | 2 |
| Uncertain significance | 0 | 86 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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10 |
![]() |
170 |
![]() |
4 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 | IL-10C |
| SYNONYM | MDA1 |
| SYNONYM | NG.1 |
| SYNONYM | ZMDA1 |
| MIM | 605687 OMIM |
| HGNC | HGNC:5990 HGNC |
| Ensembl | ENSG00000142224 Ensembl |
| AllianceGenome | HGNC:5990 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000659997.3 | hg38 | chr1 | 206,770,773 | 206,842,981 | 72,209 |
| ENST00000340758.7 | hg38 | chr1 | 206,834,363 | 206,842,979 | 8,617 |
| ENST00000656872.2 | hg38 | chr1 | 206,770,764 | 206,842,979 | 72,216 |
| ENST00000270218.10 | hg38 | chr1 | 206,828,877 | 206,842,622 | 13,746 |
| ENST00000656872.2 | hg19 | chr1 | 206,944,109 | 207,016,324 | 72,216 |
| ENST00000659997.3 | hg19 | chr1 | 206,944,118 | 207,016,326 | 72,209 |
| ENST00000270218.10 | hg19 | chr1 | 207,002,222 | 207,015,967 | 13,746 |
| ENST00000340758.7 | hg19 | chr1 | 207,007,708 | 207,016,324 | 8,617 |
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