Variant NM_000492.4:c.323C>T
Name | NM_000492.4:c.323C>T |
Protein name | NP_000483.3:p.(Ser108Phe) |
Genomic name (hg19) | chr7:g.117171002C>T UCSC gnomAD |
#Exon/intron | exon 4 |
Legacy Name | S108F |
Class | disease-causing |
Subclass | varying clinical consequence |
WT sequence | CTCTTACTGGGAAGAATCATAGCTT C CTATGACCCGGATAACAAGGAGGAA |
Mutant sequence | CTCTTACTGGGAAGAATCATAGCTT T CTATGACCCGGATAACAAGGAGGAA |
Not found | dbSNP rs397508520 |
Reference | PMID | Splicing | mRNA level | Maturation | Localization | Channel fonction (Cl-) | Bicarbonate |
Hammerle et al, 2001 | 11278813 | ✓ | ✓ | ✓ |
« ✓ » 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 | 2634 | heterozygote | varying clinical consequence- Undef |
Color code: non disease-causing < VUS1 < VUS2 < VUS3 < VUS4 < VUS5 < disease-causing |
CFTR variants are clustered into five groups: |
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