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 |

Variant on transcripts
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