SSB small RNA binding exonuclease protection factor La
Information
- Symbol
- SSB
- Type
- protein-coding
- Description
- small RNA binding exonuclease protection factor La
- Entrez Gene ID
- 6741
- Genome
- hg19
- Position
- chr2:170,655,789-170,668,574
- Genome
- hg38
- Position
- chr2:169,799,279-169,812,064
- MIM
- 109090 OMIM
- HGNC
- HGNC:11316 HGNC
- Ensembl
- ENSG00000138385 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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38 |
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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
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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 |
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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 |
---|---|
SYNONYM | LARP3 |
SYNONYM | La |
SYNONYM | La/SSB |
MIM | 109090 OMIM |
HGNC | HGNC:11316 HGNC |
Ensembl | ENSG00000138385 Ensembl |
AllianceGenome | HGNC:11316 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409333.1 | hg38 | chr2 | 169,799,279 | 169,812,064 | 12,786 |
ENST00000260956.9 | hg38 | chr2 | 169,798,871 | 169,812,064 | 13,194 |
ENST00000260956.9 | hg19 | chr2 | 170,655,381 | 170,668,574 | 13,194 |
ENST00000409333.1 | hg19 | chr2 | 170,655,789 | 170,668,574 | 12,786 |
Key | Value |
---|---|
strand | + |
start | 170,655,321 |
Gene Symbol | SSB |
Entrez GeneId | 6,741 |
Chr Band | 2q31.1 |
end | 170,668,570 |
chr | chr2 |
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