Variant #0000616435 (NC_000017.10:g.26851943C>T, NM_003593.2:c.546C>T (FOXN1))
| Chromosome |
17 |
| 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.26851943C>T |
| DNA change (hg38) |
g.28524925C>T |
| Published as |
FOXN1(NM_003593.2):c.546C>T (p.N182=) |
| ISCN |
- |
| DB-ID |
FOXN1_000012 |
| 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) |
0.00107 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2020-07-13 11:10:09 +02:00 (CEST) |

Variant on transcripts
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