LST1 leukocyte specific transcript 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 2 | 0 |
Uncertain significance | 0 | 10 |
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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 |
Search Word
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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Search word | : | |
Filtering | : |
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 | B144 |
SYNONYM | D6S49E |
SYNONYM | LST-1 |
MIM | 109170 OMIM |
HGNC | HGNC:14189 HGNC |
Ensembl | ENSG00000204482 Ensembl |
AllianceGenome | HGNC:14189 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000376090.6 | hg38 | chr6 | 31,587,022 | 31,588,909 | 1,888 |
ENST00000376093.6 | hg38 | chr6 | 31,587,200 | 31,588,909 | 1,710 |
ENST00000376092.7 | hg38 | chr6 | 31,587,200 | 31,588,662 | 1,463 |
ENST00000376099.5 | hg38 | chr6 | 31,586,217 | 31,588,909 | 2,693 |
ENST00000376096.5 | hg38 | chr6 | 31,586,217 | 31,588,909 | 2,693 |
ENST00000418507.6 | hg38 | chr6 | 31,586,124 | 31,588,909 | 2,786 |
ENST00000376089.6 | hg38 | chr6 | 31,587,054 | 31,588,909 | 1,856 |
ENST00000376086.7 | hg38 | chr6 | 31,587,200 | 31,588,908 | 1,709 |
ENST00000339530.8 | hg38 | chr6 | 31,586,699 | 31,588,810 | 2,112 |
ENST00000438075.7 | hg38 | chr6 | 31,586,277 | 31,588,909 | 2,633 |
ENST00000303757.12 | hg38 | chr6 | 31,587,200 | 31,588,909 | 1,710 |
ENST00000211921.11 | hg38 | chr6 | 31,586,848 | 31,588,810 | 1,963 |
ENST00000376110.7 | hg38 | chr6 | 31,586,220 | 31,588,757 | 2,538 |
ENST00000396101.7 | hg38 | chr6 | 31,587,300 | 31,588,909 | 1,610 |
ENST00000376096.5 | hg19 | chr6 | 31,553,994 | 31,556,686 | 2,693 |
ENST00000376099.5 | hg19 | chr6 | 31,553,994 | 31,556,686 | 2,693 |
ENST00000376110.7 | hg19 | chr6 | 31,553,997 | 31,556,534 | 2,538 |
ENST00000339530.8 | hg19 | chr6 | 31,554,476 | 31,556,587 | 2,112 |
ENST00000211921.11 | hg19 | chr6 | 31,554,625 | 31,556,587 | 1,963 |
ENST00000376093.6 | hg19 | chr6 | 31,554,977 | 31,556,686 | 1,710 |
ENST00000303757.12 | hg19 | chr6 | 31,554,977 | 31,556,686 | 1,710 |
ENST00000376090.6 | hg19 | chr6 | 31,554,799 | 31,556,686 | 1,888 |
ENST00000376089.6 | hg19 | chr6 | 31,554,831 | 31,556,686 | 1,856 |
ENST00000376086.7 | hg19 | chr6 | 31,554,977 | 31,556,685 | 1,709 |
ENST00000376092.7 | hg19 | chr6 | 31,554,977 | 31,556,439 | 1,463 |
ENST00000396101.7 | hg19 | chr6 | 31,555,077 | 31,556,686 | 1,610 |
ENST00000418507.6 | hg19 | chr6 | 31,553,901 | 31,556,686 | 2,786 |
ENST00000438075.7 | hg19 | chr6 | 31,554,054 | 31,556,686 | 2,633 |
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