Variant #0000565108 (NC_000018.9:g.53131376C>T, TCF4(NM_001083962.1):c.146-8G>A)

Chromosome 18
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.53131376C>T
DNA change (hg38) g.55464145C>T
Published as TCF4(NM_001083962.1):c.146-8G>A (p.(=))
ISCN -
DB-ID TCF4_000161
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) 0 View details
Owner VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
TCF4 NM_001083962.1 -?/. - c.146-8G>A - r.(=) p.(=)