CDRT15L2 CMT1A duplicated region transcript 15 like 2

Information
Symbol
CDRT15L2
Type
protein-coding
Description
CMT1A duplicated region transcript 15 like 2
Entrez Gene ID
256223
Genome
hg19
Position
chr17:20,483,037-20,484,224
Genome
hg38
Position
chr17:20,579,724-20,580,911
HGNC
HGNC:34075 HGNC
Ensembl
ENSG00000214819 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 1 0
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
54
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
Category :
Search word :
Filtering :
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:34075 HGNC
Ensembl ENSG00000214819 Ensembl
AllianceGenome HGNC:34075
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000661883.1 hg38 chr17 20,579,724 20,580,911 1,188
ENST00000399044.1 hg38 chr17 20,579,724 20,580,911 1,188
ENST00000399044.1 hg19 chr17 20,483,037 20,484,224 1,188
ENST00000661883.1 hg19 chr17 20,483,037 20,484,224 1,188
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