Variant #0000000681 (NC_000018.9:g.53131488C>A, TCF4(NM_001083962.1):c.146-120G>T)
Individual ID |
00000029 |
Chromosome |
18 |
Allele |
Parent #1 |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.53131488C>A |
DNA change (hg38) |
g.55464257C>A |
Published as |
- |
ISCN |
- |
DB-ID |
TCF4_000081 |
Variant remarks |
- |
Reference |
PubMed: Almomani 2011 dbSNP |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Gerard C.P. Schaafsma |

Variant on transcripts
Screenings
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