Variant #0000896281 (NC_000023.10:g.49115886T>C, NM_014008.3:c.*9164T>C (CCDC22))
| Chromosome |
X |
| Allele |
Unknown |
| 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.49115886T>C |
| DNA change (hg38) |
- |
| Published as |
FOXP3(NM_014009.3):c.-22-902A>G |
| ISCN |
- |
| DB-ID |
CCDC22_000075 |
| 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_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2022-11-01 13:41:49 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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