CHRFAM7A CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion

Information
Symbol
CHRFAM7A
Type
protein-coding
Description
CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion
Entrez Gene ID
89832
Genome
hg19
Position
chr15:30,652,769-30,685,743
Genome
hg38
Position
chr15:30,360,566-30,393,540
MIM
609756 OMIM
HGNC
HGNC:15781 HGNC
Ensembl
ENSG00000166664 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 2 0
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
26
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
SYNONYM CHRNA7
SYNONYM CHRNA7-DR1
SYNONYM D-10
SYNONYM NACHRA7
MIM 609756 OMIM
HGNC HGNC:15781 HGNC
Ensembl ENSG00000166664 Ensembl
AllianceGenome HGNC:15781
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000299847.7 hg38 chr15 30,360,566 30,393,540 32,975
ENST00000401522.7 hg38 chr15 30,362,058 30,393,360 31,303
ENST00000397827.7 hg38 chr15 30,361,240 30,393,661 32,422
ENST00000299847.7 hg19 chr15 30,652,769 30,685,743 32,975
ENST00000397827.7 hg19 chr15 30,653,443 30,685,864 32,422
ENST00000401522.7 hg19 chr15 30,654,261 30,685,563 31,303
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