ZMYND15 zinc finger MYND-type containing 15
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 8 |
| Benign | 0 | 6 |
| Likely benign | 0 | 18 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 64 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
88 |
 |
8 |
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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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 | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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 | SPGF14 |
| MIM | 614312 OMIM |
| HGNC | HGNC:20997 HGNC |
| Ensembl | ENSG00000141497 Ensembl |
| AllianceGenome | HGNC:20997 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000573751.2 | hg38 | chr17 | 4,740,519 | 4,746,116 | 5,598 |
| ENST00000269289.10 | hg38 | chr17 | 4,740,015 | 4,746,119 | 6,105 |
| ENST00000592813.5 | hg38 | chr17 | 4,740,042 | 4,746,113 | 6,072 |
| ENST00000433935.6 | hg38 | chr17 | 4,739,833 | 4,746,113 | 6,281 |
| ENST00000433935.6 | hg19 | chr17 | 4,643,128 | 4,649,408 | 6,281 |
| ENST00000269289.10 | hg19 | chr17 | 4,643,310 | 4,649,414 | 6,105 |
| ENST00000592813.5 | hg19 | chr17 | 4,643,337 | 4,649,408 | 6,072 |
| ENST00000573751.2 | hg19 | chr17 | 4,643,814 | 4,649,411 | 5,598 |
Genome browser