Variant #0000314466 (NC_000018.9:g.53298807del, TCF4(NM_001083962.1):c.-43559del)

Chromosome 18
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.53298807del
DNA change (hg38) g.55631576del
Published as TCF4(NM_001243226.2):c.196-188delA
ISCN -
DB-ID TCF4_000164
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Utrecht
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
TCF4 NM_001083962.1 -/. - c.-43559del - r.(?) p.(=)