Genomic variant #0000181947

Individual ID 00112648
Chromosome 18
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.pter_cen_(53131369_53252510)::NC_000020.10:g.(40180000_40246978)_qter
DNA change (hg38) -
Published as TCF4-CHD6 fusion
ISCN t(18;20)(q21.1;q11.2)
DB-ID TCF4_000000 See all 24 reported entries
Variant remarks fusion transcript TCF4::CHD6 ?
Reference PubMed: Kalscheuer 2008
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Genomic location of variant could not be determined
Owner Irina Giurgea




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

ClassClinical     

RNA change     

Protein     
TCF4 NM_001083962.1 +/. 3i c.145+1_146-1::NM_032221.4:c.(-24+1_-23-1) - pathogenic r.? p.?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000113106 DNA FISH - - CHD6, TCF4 4 Irina Giurgea