Variant #0000251626 (NC_000018.9:g.53131210A>T, TCF4(NM_001083962.1):c.207+97T>A)

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.53131210A>T
DNA change (hg38) g.55463979A>T
Published as TCF4(NM_001083962.1):c.207+97T>A, TCF4(NM_001243228.2):c.207+97T>A
ISCN -
DB-ID TCF4_000127 See all 2 reported entries
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.207+97T>A - r.(=) p.(=)