MYG1 MYG1 exonuclease
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 12 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
12 |
 |
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
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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 | C12orf10 |
| SYNONYM | Gamm1 |
| SYNONYM | MST024 |
| SYNONYM | MSTP024 |
| SYNONYM | MYG |
| MIM | 611366 OMIM |
| HGNC | HGNC:17590 HGNC |
| Ensembl | ENSG00000139637 Ensembl |
| AllianceGenome | HGNC:17590 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000267103.10 | hg38 | chr12 | 53,299,695 | 53,307,177 | 7,483 |
| ENST00000549488.5 | hg38 | chr12 | 53,300,093 | 53,307,177 | 7,085 |
| ENST00000548632.5 | hg38 | chr12 | 53,299,750 | 53,307,171 | 7,422 |
| ENST00000267103.10 | hg19 | chr12 | 53,693,479 | 53,700,961 | 7,483 |
| ENST00000548632.5 | hg19 | chr12 | 53,693,534 | 53,700,955 | 7,422 |
| ENST00000549488.5 | hg19 | chr12 | 53,693,877 | 53,700,961 | 7,085 |
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