ClinVar Miner

List of variants in gene combination CDCA7L, DNAH11 reported as uncertain significance

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018719.5(CDCA7L):c.*963G>C rs79947346 0.00244
NM_018719.5(CDCA7L):c.*1006A>G rs573090758 0.00092
NM_001277115.2(DNAH11):c.13548G>A (p.Ala4516=) rs147454485 0.00080
NM_001277115.2(DNAH11):c.13305C>T (p.Gly4435=) rs150682314 0.00029
NM_001277115.2(DNAH11):c.13309C>T (p.Arg4437Cys) rs200466467 0.00027
NM_001277115.2(DNAH11):c.13399G>A (p.Val4467Met) rs200609513 0.00020
NM_018719.5(CDCA7L):c.*805G>A rs192515848 0.00018
NM_018719.5(CDCA7L):c.*912A>G rs547875413 0.00017
NM_001277115.2(DNAH11):c.13346G>A (p.Arg4449His) rs138945257 0.00016
NM_001277115.2(DNAH11):c.13398C>T (p.Pro4466=) rs72658836 0.00016
NM_001277115.2(DNAH11):c.13407_13415dup (p.Gln4470_Thr4472dup) rs748080467 0.00006
NM_018719.5(CDCA7L):c.*887G>A rs886062191 0.00006
NM_001277115.2(DNAH11):c.13310G>A (p.Arg4437His) rs775606157 0.00004
NM_001277115.2(DNAH11):c.13429G>A (p.Glu4477Lys) rs551275210 0.00004
NM_018719.5(CDCA7L):c.*804C>T rs886062192 0.00004
NM_001277115.2(DNAH11):c.13351_13353del (p.Lys4451del) rs552487543 0.00003
NM_018719.5(CDCA7L):c.*942C>T rs192395057 0.00003
NM_001277115.2(DNAH11):c.13420C>A (p.Gln4474Lys) rs1467862243 0.00002
NM_001277115.2(DNAH11):c.13445G>A (p.Arg4482Lys) rs191791959 0.00002
NM_001277115.2(DNAH11):c.13445G>C (p.Arg4482Thr) rs191791959 0.00001
NM_001277115.2(DNAH11):c.13469A>T (p.Tyr4490Phe) rs1320072390 0.00001
GRCh37/hg19 7p15.3(chr7:21713059-22067069)x3
NM_001277115.2(DNAH11):c.13316A>G (p.Asp4439Gly)
NM_001277115.2(DNAH11):c.13319C>T (p.Thr4440Ile)
NM_001277115.2(DNAH11):c.13321C>G (p.Gln4441Glu)
NM_001277115.2(DNAH11):c.13325C>G (p.Ala4442Gly)
NM_001277115.2(DNAH11):c.13328G>A (p.Gly4443Glu) rs1375156859
NM_001277115.2(DNAH11):c.13331C>G (p.Thr4444Ser)
NM_001277115.2(DNAH11):c.13342G>A (p.Ala4448Thr)
NM_001277115.2(DNAH11):c.13345C>T (p.Arg4449Cys) rs751222708
NM_001277115.2(DNAH11):c.13396C>T (p.Pro4466Ser) rs1784797805
NM_001277115.2(DNAH11):c.13420C>G (p.Gln4474Glu)
NM_001277115.2(DNAH11):c.13424_13456del (p.Thr4475_Leu4485del) rs1554294443
NM_001277115.2(DNAH11):c.13429_13449dup (p.Thr4483_Lys4484insGluCysProValTyrArgThr)
NM_001277115.2(DNAH11):c.13444A>G (p.Arg4482Gly) rs1784802858
NM_001277115.2(DNAH11):c.13457G>A (p.Arg4486Lys)
NM_001277115.2(DNAH11):c.13472_*75dup (p.Ile4491_Ter4517=) rs1784806477
NM_001277115.2(DNAH11):c.13473C>G (p.Ile4491Met) rs1784806581
NM_001277115.2(DNAH11):c.13473_*75dup (p.Tyr4490_Ter4517=) rs878854439
NM_001277115.2(DNAH11):c.13475_13504dup (p.Lys4501_Thr4502insArgThrPheArgLeuLysSerGluGluLys)
NM_001277115.2(DNAH11):c.13482C>G (p.Phe4494Leu) rs370038827
NM_001277115.2(DNAH11):c.13499A>G (p.Glu4500Gly)
NM_001277115.2(DNAH11):c.13500_13504del (p.Glu4500fs) rs72658839
NM_001277115.2(DNAH11):c.13515_13526dup (p.Leu4507_Val4510dup) rs1254126467
NM_001277115.2(DNAH11):c.13523_13543dup (p.Ala4508_Leu4514dup) rs1784814248
NM_001277115.2(DNAH11):c.13527_13547dup (p.Val4510_Ala4516dup) rs1784815114
NM_001277115.2(DNAH11):c.13531G>A (p.Ala4511Thr) rs1562614917
NM_001277115.2(DNAH11):c.13536_13548dup (p.Ter4517AlaextTer?) rs764221599
NM_001277115.2(DNAH11):c.13537C>A (p.Leu4513Ile)
NM_018719.5(CDCA7L):c.*766_*769dup rs745609865
NM_018719.5(CDCA7L):c.*788T>C rs1289391313
NM_018719.5(CDCA7L):c.*875G>A rs72658842
NM_018719.5(CDCA7L):c.*918_*919dup rs886062190
NM_018719.5(CDCA7L):c.*989G>A rs886062189

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.