SMIM2-IT1 SMIM2 intronic transcript 1
Information
- Symbol
- SMIM2-IT1
- Type
- ncRNA
- Description
- SMIM2 intronic transcript 1
- Entrez Gene ID
- 100874377
- Genome
- hg19
- Position
- chr13:44,720,606-44,732,358
- Genome
- hg38
- Position
- chr13:44,146,470-44,158,222
- HGNC
- HGNC:41492 HGNC
- Ensembl
- ENSG00000235285 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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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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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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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 | C13orf44-IT1 |
HGNC | HGNC:41492 HGNC |
Ensembl | ENSG00000235285 Ensembl |
AllianceGenome | HGNC:41492 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000415082.1 | hg38 | chr13 | 44,146,470 | 44,158,222 | 11,753 |
ENST00000415082.1 | hg19 | chr13 | 44,720,606 | 44,732,358 | 11,753 |
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