Variant #0000211214 (NC_000018.9:g.52928697C>T, NM_001083962.1:c.990G>A (TCF4))

Chromosome 18
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.52928697C>T
DNA change (hg38) g.55261466C>T
Published as -
ISCN -
DB-ID TCF4_000098 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Irina Giurgea
Database submission license No license selected
Created by Irina Giurgea
Date created 2017-09-11 20:10:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
TCF4 NM_001083962.1 ./. 12 c.990G>A - r.(=) p.(=)


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