LASP1 LIM and SH3 protein 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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26 |
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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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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 | Lasp-1 |
SYNONYM | MLN50 |
MIM | 602920 OMIM |
HGNC | HGNC:6513 HGNC |
Ensembl | ENSG00000002834 Ensembl |
AllianceGenome | HGNC:6513 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000433206.6 | hg38 | chr17 | 38,869,859 | 38,921,769 | 51,911 |
ENST00000318008.11 | hg38 | chr17 | 38,870,058 | 38,921,770 | 51,713 |
ENST00000433206.6 | hg19 | chr17 | 37,026,112 | 37,078,022 | 51,911 |
ENST00000318008.11 | hg19 | chr17 | 37,026,311 | 37,078,023 | 51,713 |
Key | Value |
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strand | + |
start | 37,026,111 |
Gene Symbol | LASP1 |
Entrez GeneId | 3,927 |
Chr Band | 17q11-q21.3 |
end | 37,078,022 |
chr | chr17 |
Name | LIM and SH3 protein 1 |
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