Genomic variant #0000064419

Individual ID 00037224
Chromosome 18
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.52928807C>T
DNA change (hg38) g.55261576C>T
Published as -
ISCN -
DB-ID TCF4_000088 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs35918540
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.02776 View details
Owner Andreas Laner
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

ClassClinical     

RNA change     

Protein     
TCF4 NM_001083962.1 -/. - c.923-43G>A - - r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000037294 DNA SEQ - - TCF4 1 Andreas Laner