Variant NM_000492.4:c.489+76T>C
Name | NM_000492.4:c.489+76T>C |
Protein name | NP_000483.3:p.(=) |
Genomic name (hg19) | chr7:g.117171244T>C UCSC gnomAD |
#Exon/intron | intron 4 |
Class | VUS |
Subclass | VUS3 |
WT sequence | TGTTTTAATGTCATAAATTAGGTAG T GAGCTGGTACAAGTAAGGGATAAAT |
Mutant sequence | TGTTTTAATGTCATAAATTAGGTAG C GAGCTGGTACAAGTAAGGGATAAAT |
Not found | Not found | dbSNP no rs | Not found |
No patient found in CFTR-NGS catalogue |
TOTAL NUMBER OF PATIENTS | 1 |
---|---|
CFTR-RD | 1
|
Phenotype | Patient ID | Variant status | Additional variants |
---|---|---|---|
Bronchiectasis | 4773 | heterozygote | CFTR-RD-causing- Undef CF-causing- Undef VUS1- Undef |
Color code: non disease-causing < VUS1 < VUS2 < VUS3 < VUS4 < VUS5 < disease-causing |
CFTR variants are clustered into five groups: |
|