CFTR-NGS variants catalogue
Variant hg19:chr7:117303563T/TA
Name | NM_000492.4:c.3964-1161dupA |
Protein name | NP_000483.3:p.(?) |
Genomic name (hg19) | chr7:g.117303581dup UCSC |
#Exon/intron | intron 24 |
Type in CFTR-NGS catalogue | repeat |
Class in CFTR-France | not reported |
WT sequence | TCCAGCTAAAAAAAAAAAAAAAAAA - CAAGCCATTGGTCCTAACACAACTT |
Mutant sequence | TCCAGCTAAAAAAAAAAAAAAAAAA A CAAGCCATTGGTCCTAACACAACTT |
MAF (GnomAD) | 8.63e-03 |
Splicing prediction (SpliceAI) | AG: 0.00 (-1) AL: 0.00 (23) DG: 0.00 (-34) DL: 0.00 (-30) |
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 | 4 |
---|---|
CF | 3 |
CFTR-RD | 1
|
ID | Phenotype | Laboratory | Experiment | Variant status | Variant filter | Quality score | Depth of coverage |
---|---|---|---|---|---|---|---|
21 | CF | Montpellier | 150517_varilh | heterozygous | PASS | 1226 | 466 |
22 | CF | Montpellier | 150517_varilh | heterozygous | PASS | 1673 | 422 |
9879 | CF | Montpellier | 160218_varilh | heterozygous | PASS | 1028 | 328 |
6008 | CFTR-RD | Montpellier | 160218_varilh | heterozygous | PASS | 967 | 317 |