Variant #0000620657 (NC_000001.10:g.47882321C>T, NM_012186.2:c.334C>T (FOXE3))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47882321C>T |
| DNA change (hg38) |
g.47416649C>T |
| Published as |
FOXE3(NM_012186.2):c.334C>T (p.P112S), FOXE3(NM_012186.3):c.334C>T (p.P112S) |
| ISCN |
- |
| DB-ID |
FOXE3_000043 See all 2 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
4.0E-5 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-12-06 12:43:26 +01:00 (CET) |
| Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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