Variant #0000273329 (NC_000007.13:g.117199522C>G, NM_000492.3:c.1397C>G (CFTR))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.117199522C>G |
| DNA change (hg38) |
g.117559468C>G |
| Published as |
CFTR(NM_000492.3):c.1397C>G (p.S466*) |
| ISCN |
- |
| DB-ID |
CFTR_001108 See all 5 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) |
1.0E-5 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-06-23 13:58:20 +02:00 (CEST) |

Variant on transcripts
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