SNRNP25 small nuclear ribonucleoprotein U11/U12 subunit 25
Information
- Symbol
- SNRNP25
- Type
- protein-coding
- Description
- small nuclear ribonucleoprotein U11/U12 subunit 25
- Entrez Gene ID
- 79622
- Genome
- hg19
- Position
- chr16:103,828-107,669
- Genome
- hg38
- Position
- chr16:53,828-57,669
- HGNC
- HGNC:14161 HGNC
- Ensembl
- ENSG00000161981 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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16 |
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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
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
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 |
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | C16orf33 |
HGNC | HGNC:14161 HGNC |
Ensembl | ENSG00000161981 Ensembl |
AllianceGenome | HGNC:14161 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000293861.8 | hg38 | chr16 | 53,828 | 57,669 | 3,842 |
ENST00000710415.1 | hg38 | chr16 | 53,828 | 57,669 | 3,842 |
ENST00000293861.8 | hg19 | chr16 | 103,828 | 107,669 | 3,842 |
ENST00000710415.1 | hg19 | chr16 | 103,828 | 107,669 | 3,842 |
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