Variant #0001047713 (NC_000007.13:g.117144344C>T, NM_000492.3:c.91C>T (CFTR))
Chromosome |
7 |
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.117144344C>T |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
CFTR_000125 See all 4 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs1800073 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00165 View details |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2025-09-05 16:08:01 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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