Variant #0000518068 (NC_000003.11:g.138664911G>A, NM_023067.3:c.654C>T (FOXL2))
| Chromosome |
3 |
| 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.138664911G>A |
| DNA change (hg38) |
g.138946069G>A |
| Published as |
FOXL2(NM_023067.4):c.654C>T (p.C218=) |
| ISCN |
- |
| DB-ID |
C3orf72_000004 |
| 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) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-06-15 16:07:15 +02:00 (CEST) |

Variant on transcripts
|