Variant #0000311765 (NC_000018.9:g.53128354T>C, TCF4(NM_001083962.1):c.208-8A>G)

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.53128354T>C
DNA change (hg38) g.55461123T>C
Published as TCF4(NM_001083962.1):c.208-8A>G
ISCN -
DB-ID TCF4_000125
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) 0.00049 View details
Owner VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
TCF4 NM_001083962.1 -?/. - c.208-8A>G - r.(=) p.(=)