ClinVar Miner

List of variants reported as uncertain significance for squamous cell lung carcinoma by Faculté Pluridciplinaire Nador, Université Mohamed Premier

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 41
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006182.4(DDR2):c.1856+32G>T rs1355287 0.99589
NM_006182.4(DDR2):c.1504+25T>C rs1780003 0.95433
NM_000077.5(CDKN2A):c.*29G>C rs11515 0.85710
NM_003537.4(H3C2):c.*10C>T rs2213284 0.75855
NM_006206.6(PDGFRA):c.2440-50_2440-49insA rs3830355 0.75180
NM_000222.3(KIT):c.2484+78T>C rs1008658 0.52503
NM_058195.4(CDKN2A):c.194-3810G>A rs3814960 0.49402
NM_000455.5(STK11):c.375-49G>A rs34928889 0.45190
NM_000455.5(STK11):c.465-51T>C rs2075606 0.29935
NM_002755.4(MAP2K1):c.291+22G>C rs16949924 0.27222
NM_004304.5(ALK):c.3359+24G>C rs2276550 0.26990
NM_006218.4(PIK3CA):c.352+40A>G rs3729674 0.26066
NM_004304.5(ALK):c.4165-6C>T rs17007646 0.20768
NM_000455.5(STK11):c.374+24G>T rs2075604 0.18985
NM_000141.5(FGFR2):c.1864-43del rs111564057 0.17733
NM_006218.4(PIK3CA):c.1540-55C>T rs45455192 0.04697
NM_006182.4(DDR2):c.1505-19G>A rs143729297 0.00789
NM_000222.3(KIT):c.2597-51T>C rs368272654 0.00263
NM_000142.5(FGFR3):c.1266+25C>T rs200827273 0.00088
NC_000006.12:g.26032121C>G rs184952244 0.00080
NM_005343.4(HRAS):c.450+35A>C rs749486358 0.00012
NM_000141.5(FGFR2):c.1986+23G>C rs1845634185
NM_000142.5(FGFR3):c.1837-3C>T rs1721872448
NM_000245.4(MET):c.2265-118del rs1794304820
NM_000314.8(PTEN):c.634+14A>G rs762694325
NM_000455.5(STK11):c.464+44dup rs544282452
NM_000455.5(STK11):c.464+95T>C rs2080767432
NM_000455.5(STK11):c.598-32C>T rs2080775539
NM_004304.5(ALK):c.3451-35TCC[3] rs775243091
NM_004304.5(ALK):c.3744-53del rs1669420011
NM_004304.5(ALK):c.4165-19del rs1668958808
NM_004985.5(KRAS):c.291-50A>G rs1951385786
NM_005343.4(HRAS):c.111+18G>C rs759743352
NM_005343.4(HRAS):c.450+31A>G rs1300614609
NM_005343.4(HRAS):c.450+38dup rs1851232069
NM_006182.4(DDR2):c.1099+20T>C rs1663742530
NM_006182.4(DDR2):c.2434-46TC[6] rs555765842
NM_006182.4(DDR2):c.2434-46TC[7] rs555765842
NM_006182.4(DDR2):c.2434-46TC[9] rs555765842
NM_006218.4(PIK3CA):c.562+40del rs1724368987
NM_058195.4(CDKN2A):c.194-3838A>G rs1819982421

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.