TSEN15 tRNA splicing endonuclease subunit 15
Information
- Symbol
- TSEN15
- Type
- protein-coding
- Description
- tRNA splicing endonuclease subunit 15
- Entrez Gene ID
- 116461
- Genome
- hg19
- Position
- chr1:184,020,810-184,043,340
- Genome
- hg38
- Position
- chr1:184,051,676-184,074,206
- MIM
- 608756 OMIM
- HGNC
- HGNC:16791 HGNC
- Ensembl
- ENSG00000198860 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 22 |
Likely benign | 0 | 24 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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78 |
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2 |
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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
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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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 | C1orf19 |
SYNONYM | PCH2F |
SYNONYM | sen15 |
MIM | 608756 OMIM |
HGNC | HGNC:16791 HGNC |
Ensembl | ENSG00000198860 Ensembl |
AllianceGenome | HGNC:16791 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000361641.6 | hg38 | chr1 | 184,051,676 | 184,074,206 | 22,531 |
ENST00000643231.1 | hg38 | chr1 | 184,051,686 | 184,097,485 | 45,800 |
ENST00000533373.6 | hg38 | chr1 | 184,051,699 | 184,074,212 | 22,514 |
ENST00000647465.1 | hg38 | chr1 | 184,051,718 | 184,095,845 | 44,128 |
ENST00000645963.2 | hg38 | chr1 | 184,051,756 | 184,095,845 | 44,090 |
ENST00000423085.7 | hg38 | chr1 | 184,051,651 | 184,074,212 | 22,562 |
ENST00000647437.1 | hg38 | chr1 | 184,051,712 | 184,074,127 | 22,416 |
ENST00000645668.2 | hg38 | chr1 | 184,051,730 | 184,074,212 | 22,483 |
ENST00000361641.6 | hg19 | chr1 | 184,020,810 | 184,043,340 | 22,531 |
ENST00000423085.7 | hg19 | chr1 | 184,020,785 | 184,043,346 | 22,562 |
ENST00000643231.1 | hg19 | chr1 | 184,020,820 | 184,066,619 | 45,800 |
ENST00000533373.6 | hg19 | chr1 | 184,020,833 | 184,043,346 | 22,514 |
ENST00000645668.2 | hg19 | chr1 | 184,020,864 | 184,043,346 | 22,483 |
ENST00000645963.2 | hg19 | chr1 | 184,020,890 | 184,064,979 | 44,090 |
ENST00000647437.1 | hg19 | chr1 | 184,020,846 | 184,043,261 | 22,416 |
ENST00000647465.1 | hg19 | chr1 | 184,020,852 | 184,064,979 | 44,128 |
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