SCGB1D1 secretoglobin family 1D member 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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12 |
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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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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 |
Search Word
Target data | : |
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 | LIPA |
SYNONYM | LPHA |
SYNONYM | LPNA |
MIM | 615060 OMIM |
HGNC | HGNC:18395 HGNC |
Ensembl | ENSG00000168515 Ensembl |
AllianceGenome | HGNC:18395 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000306238.3 | hg38 | chr11 | 62,190,216 | 62,193,539 | 3,324 |
ENST00000306238.3 | hg19 | chr11 | 61,957,688 | 61,961,011 | 3,324 |
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