CFTR-NGS variants catalogue
Variant hg19:chr7:117136847CATTGTGTGAGT/C
Name | NM_000492.4:c.54-7459_54-7449del11 |
Protein name | NP_000483.3:p.(?) |
Genomic name (hg19) | chr7:g.117136848_117136858del UCSC |
#Exon/intron | intron 1 |
Type in CFTR-NGS catalogue | - |
Class in CFTR-France | not reported |
WT sequence | TGCATCATTTTAAATTCCTTCCACC ATTGTGTGAGT GTTTCAATTTCTCCACATATTTGCA |
Mutant sequence | TGCATCATTTTAAATTCCTTCCACC ----------- GTTTCAATTTCTCCACATATTTGCA |
MAF (GnomAD) | - |
Splicing prediction (SpliceAI) | - |
Not found | Not found | dbSNP no rs | Not found |
Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
not verified | not performed |
No patient found in CFTR-France |
TOTAL NUMBER OF INDIVIDUALS | 1 |
---|---|
Asymptomatic | 1 |
ID | Phenotype | Laboratory | Experiment | Variant status | Variant filter | Quality score | Depth of coverage |
---|---|---|---|---|---|---|---|
MUCO07168 | Asymptomatic | Montpellier | 100714_varilh | heterozygous | alleleBias | 39 | 0 |