CFTR-NGS variants catalogue
Variant hg19:chr7:117257673A/G
Name | NM_000492.4:c.3468+2906A>G |
Protein name | NP_000483.3:p.(?) |
Genomic name (hg19) | chr7:g.117257673A>G UCSC gnomAD |
#Exon/intron | intron 21 |
Type in CFTR-NGS catalogue | - |
Class in CFTR-France | not reported |
Patients reported in CFTR-NGS, carrying this variant also carry: |