CFTR-NGS variants catalogue
Variant hg19:chr7:117252077G/GTA
Name | NM_000492.4:c.3367+244_3367+245dupTA |
Protein name | NP_000483.3:p.(?) |
Genomic name (hg19) | chr7:g.117252106_117252107dup UCSC |
#Exon/intron | intron 20 |
Type in CFTR-NGS catalogue | microsatellite |
Class in CFTR-France | not reported |
Patients reported in CFTR-NGS, carrying this variant also carry: |