Variant NM_000492.4:c.2754T>G
Name | NM_000492.4:c.2754T>G |
Protein name | NP_000483.3:p.(Ile918Met) |
Genomic name (hg19) | chr7:g.117243682T>G UCSC gnomAD |
#Exon/intron | exon 17 |
Legacy Name | I918M |
Class | VUS |
Subclass | VUS4 |
WT sequence | CCAGTTCGTATTATGTGTTTTACAT T TACGTGGGAGTAGCCGACACTTTGC |
Mutant sequence | CCAGTTCGTATTATGTGTTTTACAT G TACGTGGGAGTAGCCGACACTTTGC |
Not found | dbSNP rs397508429 |
Reference | PMID | Splicing | mRNA level | Maturation | Localization | Channel fonction (Cl-) | Bicarbonate |
Bergougnoux et al, 2022 | 36567205 | ✓ | ✓ | ✓ | ✓ | ✓ |
« ✓ » indicates the type of analysis performed and not the results
Color code: non disease-causing < VUS1 < VUS2 < VUS3 < VUS4 < VUS5 < disease-causing |
No patient found in CFTR-NGS catalogue |
TOTAL NUMBER OF PATIENTS | 1 |
---|---|
CFTR-RD | 1
|
Phenotype | Patient ID | Variant status | Additional variants |
---|---|---|---|
CBAVD | 1399 | heterozygote | CFTR-RD-causing - Cis CF-causing - Trans |
Color code: non disease-causing < VUS1 < VUS2 < VUS3 < VUS4 < VUS5 < disease-causing |
CFTR variants are clustered into five groups: |
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