SNORD12 small nucleolar RNA, C/D box 12
Information
- Symbol
- SNORD12
- Type
- snoRNA
- Description
- small nucleolar RNA, C/D box 12
- Entrez Gene ID
- 692057
- Genome
- hg19
- Position
- chr20:47,897,220-47,897,309
- Genome
- hg38
- Position
- chr20:49,280,683-49,280,772
- HGNC
- HGNC:32708 HGNC
- Ensembl
- ENSG00000212304 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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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 | |||||
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | HBII-99 |
SYNONYM | MIR1259 |
SYNONYM | MIRN1259 |
HGNC | HGNC:32708 HGNC |
Ensembl | ENSG00000212304 Ensembl |
AllianceGenome | HGNC:32708 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000391002.1 | hg38 | chr20 | 49,280,683 | 49,280,772 | 90 |
ENST00000391002.1 | hg19 | chr20 | 47,897,220 | 47,897,309 | 90 |
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