Variant #0000658417 (NC_000018.9:g.53177774G>C, TCF4(NM_001083962.1):c.146-46406C>G)

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.53177774G>C
DNA change (hg38) g.55510543G>C
Published as TCF4(NM_001243228.2):c.146-46406C>G
ISCN -
DB-ID TCF4_000176
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) 0.34014 View details
Owner VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
TCF4 NM_001083962.1 -/. - c.146-46406C>G - r.(=) p.(=)