Variant #0000658414 (NC_000018.9:g.53128330G>C, TCF4(NM_001083962.1):c.224C>G)

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.53128330G>C
DNA change (hg38) g.55461099G>C
Published as TCF4(NM_001243228.2):c.224C>G (p.T75S)
ISCN -
DB-ID TCF4_000174
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) Variant not found in online data sets
Owner VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
TCF4 NM_001083962.1 ?/. - c.224C>G - r.(?) p.(Thr75Ser)