TRMT2B tRNA methyltransferase 2 homolog B
Information
- Symbol
- TRMT2B
- Type
- protein-coding
- Description
- tRNA methyltransferase 2 homolog B
- Entrez Gene ID
- 79979
- Genome
- hg19
- Position
- chrX:100,264,339-100,307,100
- Genome
- hg38
- Position
- chrX:101,009,350-101,052,111
- HGNC
- HGNC:25748 HGNC
- Ensembl
- ENSG00000188917 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 6 | 0 |
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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26 |
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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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | CXorf34 |
SYNONYM | dJ341D10.3 |
HGNC | HGNC:25748 HGNC |
Ensembl | ENSG00000188917 Ensembl |
AllianceGenome | HGNC:25748 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000545398.5 | hg38 | chrX | 101,009,346 | 101,052,116 | 42,771 |
ENST00000372935.5 | hg38 | chrX | 101,009,542 | 101,052,070 | 42,529 |
ENST00000372936.4 | hg38 | chrX | 101,009,350 | 101,052,111 | 42,762 |
ENST00000372939.5 | hg38 | chrX | 101,009,350 | 101,052,054 | 42,705 |
ENST00000545398.5 | hg19 | chrX | 100,264,335 | 100,307,105 | 42,771 |
ENST00000372939.5 | hg19 | chrX | 100,264,339 | 100,307,043 | 42,705 |
ENST00000372936.4 | hg19 | chrX | 100,264,339 | 100,307,100 | 42,762 |
ENST00000372935.5 | hg19 | chrX | 100,264,531 | 100,307,059 | 42,529 |
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