Variant #0000358074 (NC_000018.9:g.53210302=, TCF4(NM_001083962.1):c.145+42209=)
Individual ID |
00155304 |
Chromosome |
18 |
Allele |
Parent #1 |
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.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 (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Johan den Dunnen |

Variant on transcripts
Screenings
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