Variant NM_000492.4:c.4242_4242+1delinsTT
Name | NM_000492.4:c.4242_4242+1delinsTT |
Protein name | NP_000483.3:p.? |
Genomic name (hg19) | chr7:g.117305618_117305619delinsTT UCSC |
#Exon/intron | exon 26 |
Legacy Name | 4374_4374+1GG>TT |
Class | VUS |
Subclass | VUS3 |
WT sequence | CAATGCTGGAATGCCAACAATTTTT GG TGAGTCTTTATAACTTTACTTAAGA |
Mutant sequence | CAATGCTGGAATGCCAACAATTTTT TT TGAGTCTTTATAACTTTACTTAAGA |
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 |
---|---|---|---|
CBAVD | 659 | heterozygote | CFTR-RD-causing- Undef CFTR-RD-causing- Undef CFTR-RD-causing- Undef |
Color code: non disease-causing < VUS1 < VUS2 < VUS3 < VUS4 < VUS5 < disease-causing |
CFTR variants are clustered into five groups: |
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