SNORD12C small nucleolar RNA, C/D box 12C
Information
- Symbol
- SNORD12C
- Type
- snoRNA
- Description
- small nucleolar RNA, C/D box 12C
- Entrez Gene ID
- 26765
- Genome
- hg19
- Position
- chr20:47,895,477-47,895,565
- Genome
- hg38
- Position
- chr20:49,278,940-49,279,028
- HGNC
- HGNC:10105 HGNC
- Ensembl
- ENSG00000209042 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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Filtering | : |
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 | E2 |
SYNONYM | E2-1 |
SYNONYM | E3 |
SYNONYM | RNU106 |
SYNONYM | SNORD106 |
SYNONYM | U106 |
HGNC | HGNC:10105 HGNC |
Ensembl | ENSG00000209042 Ensembl |
AllianceGenome | HGNC:10105 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000386307.1 | hg38 | chr20 | 49,278,940 | 49,279,028 | 89 |
ENST00000386307.1 | hg19 | chr20 | 47,895,477 | 47,895,565 | 89 |
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