SCGB2B2 secretoglobin family 2B member 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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24 |
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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
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 |
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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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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 | SCGB4A2 |
SYNONYM | SCGBL |
MIM | 615063 OMIM |
HGNC | HGNC:27616 HGNC |
Ensembl | ENSG00000205209 Ensembl |
AllianceGenome | HGNC:27616 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000601241.6 | hg38 | chr19 | 34,590,644 | 34,677,159 | 86,516 |
ENST00000379204.2 | hg38 | chr19 | 34,593,442 | 34,594,585 | 1,144 |
ENST00000601241.6 | hg19 | chr19 | 35,081,549 | 35,168,064 | 86,516 |
ENST00000379204.2 | hg19 | chr19 | 35,084,347 | 35,085,490 | 1,144 |
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