NDUFC2-KCTD14 NDUFC2-KCTD14 readthrough

Information
Symbol
NDUFC2-KCTD14
Type
protein-coding
Description
NDUFC2-KCTD14 readthrough
Entrez Gene ID
100532726
Genome
hg19
Position
chr11:77,728,221-77,790,819
Genome
hg38
Position
chr11:78,017,175-78,079,773
HGNC
HGNC:42956 HGNC
Ensembl
ENSG00000259112 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Benign 0 2
Likely benign 0 4
not provided 1 0
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
46
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:42956 HGNC
Ensembl ENSG00000259112 Ensembl
AllianceGenome HGNC:42956
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000612612.5 hg38 chr11 78,017,175 78,079,773 62,599
ENST00000614236.2 hg38 chr11 78,017,175 78,079,773 62,599
ENST00000530054.1 hg38 chr11 78,017,046 78,079,865 62,820
ENST00000528251.1 hg38 chr11 78,016,971 78,079,844 62,874
ENST00000528251.1 hg19 chr11 77,728,017 77,790,890 62,874
ENST00000530054.1 hg19 chr11 77,728,092 77,790,911 62,820
ENST00000612612.5 hg19 chr11 77,728,221 77,790,819 62,599
ENST00000614236.2 hg19 chr11 77,728,221 77,790,819 62,599
Genome browser