ETV3L ETS variant transcription factor 3 like

Information
Symbol
ETV3L
Type
protein-coding
Description
ETS variant transcription factor 3 like
Entrez Gene ID
440695
Genome
hg19
Position
chr1:157,061,835-157,069,600
Genome
hg38
Position
chr1:157,092,043-157,099,808
HGNC
HGNC:33834 HGNC
Ensembl
ENSG00000253831 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 22
Uncertain significance 0 46
Ranking
ClinVar
0
0
2
74
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
Category :
Search word :
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Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
HGNC HGNC:33834 HGNC
Ensembl ENSG00000253831 Ensembl
AllianceGenome HGNC:33834
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000671886.1 hg38 chr1 157,092,043 157,112,357 20,315
ENST00000671942.1 hg38 chr1 157,092,043 157,112,412 20,370
ENST00000454449.3 hg38 chr1 157,092,043 157,099,808 7,766
ENST00000672100.1 hg38 chr1 157,092,043 157,112,412 20,370
ENST00000454449.3 hg19 chr1 157,061,835 157,069,600 7,766
ENST00000671886.1 hg19 chr1 157,061,835 157,082,149 20,315
ENST00000671942.1 hg19 chr1 157,061,835 157,082,204 20,370
ENST00000672100.1 hg19 chr1 157,061,835 157,082,204 20,370
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