MIR7515HG MIR7515 host gene
Information
- Symbol
- MIR7515HG
- Type
- ncRNA
- Description
- MIR7515 host gene
- Entrez Gene ID
- 102800314
- Genome
- hg19
- Position
- chr2:6,757,334-6,790,671
- Genome
- hg38
- Position
- chr2:6,617,202-6,650,539
- HGNC
- HGNC:49838 HGNC
- Ensembl
- ENSG00000236172 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 6 | 0 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
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0 |
 |
0 |
 |
0 |
 |
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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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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 | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| 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
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| Category | : |
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| 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 | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000630510.1 | hg38 | chr2 | 6,636,399 | 6,638,291 | 1,893 |
| ENST00000656553.1 | hg38 | chr2 | 6,633,997 | 6,650,525 | 16,529 |
| ENST00000588108.5 | hg38 | chr2 | 6,633,838 | 6,638,748 | 4,911 |
| ENST00000585872.5 | hg38 | chr2 | 6,632,322 | 6,635,594 | 3,273 |
| ENST00000663783.1 | hg38 | chr2 | 6,617,202 | 6,650,539 | 33,338 |
| ENST00000590865.6 | hg38 | chr2 | 6,618,268 | 6,650,501 | 32,234 |
| ENST00000592565.5 | hg38 | chr2 | 6,617,814 | 6,633,923 | 16,110 |
| ENST00000591053.5 | hg38 | chr2 | 6,632,460 | 6,636,163 | 3,704 |
| ENST00000586753.5 | hg38 | chr2 | 6,617,656 | 6,633,822 | 16,167 |
| ENST00000593269.5 | hg38 | chr2 | 6,636,061 | 6,638,805 | 2,745 |
| ENST00000590961.5 | hg38 | chr2 | 6,633,869 | 6,635,823 | 1,955 |
| ENST00000585718.6 | hg38 | chr2 | 6,633,554 | 6,650,486 | 16,933 |
| ENST00000625915.2 | hg38 | chr2 | 6,615,790 | 6,633,948 | 18,159 |
| ENST00000585718.6 | hg19 | chr2 | 6,773,686 | 6,790,618 | 16,933 |
| ENST00000588108.5 | hg19 | chr2 | 6,773,970 | 6,778,880 | 4,911 |
| ENST00000586753.5 | hg19 | chr2 | 6,757,788 | 6,773,954 | 16,167 |
| ENST00000585872.5 | hg19 | chr2 | 6,772,454 | 6,775,726 | 3,273 |
| ENST00000590865.6 | hg19 | chr2 | 6,758,400 | 6,790,633 | 32,234 |
| ENST00000590961.5 | hg19 | chr2 | 6,774,001 | 6,775,955 | 1,955 |
| ENST00000592565.5 | hg19 | chr2 | 6,757,946 | 6,774,055 | 16,110 |
| ENST00000591053.5 | hg19 | chr2 | 6,772,592 | 6,776,295 | 3,704 |
| ENST00000625915.2 | hg19 | chr2 | 6,755,922 | 6,774,080 | 18,159 |
| ENST00000663783.1 | hg19 | chr2 | 6,757,334 | 6,790,671 | 33,338 |
| ENST00000630510.1 | hg19 | chr2 | 6,776,531 | 6,778,423 | 1,893 |
| ENST00000656553.1 | hg19 | chr2 | 6,774,129 | 6,790,657 | 16,529 |
| ENST00000593269.5 | hg19 | chr2 | 6,776,193 | 6,778,937 | 2,745 |
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