Genomic variant #0000358086

Individual ID 00155308
Chromosome 18
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.53210302=
DNA change (hg38) g.55543071=
Published as rs613872 G
ISCN -
DB-ID TCF4_000151 See all 6 reported entries
Variant remarks -
Reference PubMed: Mootha 2014
ClinVar ID -
dbSNP ID rs613872
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Johan den Dunnen




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

ClassClinical     

RNA change     

Protein     
TCF4 NM_001083962.1 -/. 3i c.145+42209= - benign r.(?) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000156172 DNA PCRrp - - TCF4 3 Johan den Dunnen