SSTR3 somatostatin receptor 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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66 |
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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
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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 |
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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 |
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SYNONYM | SS-3-R |
SYNONYM | SS3-R |
SYNONYM | SS3R |
SYNONYM | SSR-28 |
SYNONYM | SST3 |
MIM | 182453 OMIM |
HGNC | HGNC:11332 HGNC |
Ensembl | ENSG00000278195 Ensembl |
AllianceGenome | HGNC:11332 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000610913.2 | hg38 | chr22 | 37,204,237 | 37,212,477 | 8,241 |
ENST00000617123.1 | hg38 | chr22 | 37,206,480 | 37,210,965 | 4,486 |
ENST00000610913.2 | hg19 | chr22 | 37,600,277 | 37,608,517 | 8,241 |
ENST00000617123.1 | hg19 | chr22 | 37,602,520 | 37,607,005 | 4,486 |
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