ClinVar Miner

List of variants in gene DNHD1 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_144666.3(DNHD1):c.1865A>C (p.Asp622Ala) rs4633449 0.67496
NM_144666.3(DNHD1):c.2090A>G (p.Gln697Arg) rs2344828 0.67355
NM_144666.3(DNHD1):c.2081A>G (p.Asn694Ser) rs7480644 0.67011
NM_144666.3(DNHD1):c.2305G>A (p.Gly769Arg) rs2344829 0.66146
NM_144666.3(DNHD1):c.1252C>T (p.His418Tyr) rs4758423 0.27376
NM_144666.3(DNHD1):c.2536C>A (p.Leu846Met) rs4282961 0.26633
NM_144666.3(DNHD1):c.7120G>A (p.Val2374Met) rs11606889 0.15661
NM_144666.3(DNHD1):c.14244C>T (p.Cys4748=) rs7129801 0.03077
NM_144666.3(DNHD1):c.1482C>T (p.Tyr494=) rs114704893 0.00958
NM_144666.3(DNHD1):c.9122T>C (p.Ile3041Thr) rs116327405 0.00885
NM_144666.3(DNHD1):c.11908A>G (p.Ser3970Gly) rs182100916 0.00854
NM_144666.3(DNHD1):c.6664C>T (p.Arg2222Cys) rs145678295 0.00748
NM_144666.3(DNHD1):c.4080C>G (p.Phe1360Leu) rs149570530 0.00716
NM_144666.3(DNHD1):c.2561G>A (p.Arg854Gln) rs75796419 0.00656
NM_144666.3(DNHD1):c.5657G>A (p.Arg1886Gln) rs147597453 0.00647
NM_144666.3(DNHD1):c.6064G>C (p.Gly2022Arg) rs184654382 0.00644
NM_144666.3(DNHD1):c.3246G>A (p.Glu1082=) rs118078642 0.00614
NM_144666.3(DNHD1):c.7295G>A (p.Gly2432Asp) rs147442229 0.00554
NM_144666.3(DNHD1):c.9G>A (p.Pro3=) rs117055865 0.00554
NM_144666.3(DNHD1):c.11420C>T (p.Pro3807Leu) rs76457785 0.00521
NM_144666.3(DNHD1):c.8960T>C (p.Leu2987Pro) rs116082386 0.00516
NM_144666.3(DNHD1):c.9639G>A (p.Leu3213=) rs145612158 0.00516
NM_144666.3(DNHD1):c.7623T>C (p.Pro2541=) rs114809425 0.00504
NM_144666.3(DNHD1):c.13068A>C (p.Thr4356=) rs11603359 0.00456
NM_144666.3(DNHD1):c.1086A>G (p.Pro362=) rs77615924 0.00411
NM_144666.3(DNHD1):c.9895C>A (p.Leu3299Met) rs74053420 0.00385
NM_144666.3(DNHD1):c.1323C>T (p.Ala441=) rs149380422 0.00376
NM_144666.3(DNHD1):c.9463G>A (p.Gly3155Ser) rs189381995 0.00359
NM_144666.3(DNHD1):c.5793G>A (p.Leu1931=) rs200466112 0.00357
NM_144666.3(DNHD1):c.9598G>C (p.Glu3200Gln) rs200787537 0.00316
NM_144666.3(DNHD1):c.6624G>A (p.Gln2208=) rs181755942 0.00307
NM_144666.3(DNHD1):c.1392+9C>G rs144297192 0.00263
NM_144666.3(DNHD1):c.4060G>A (p.Ala1354Thr) rs200542540 0.00257
NM_144666.3(DNHD1):c.1134G>C (p.Lys378Asn) rs150652653 0.00252
NM_144666.3(DNHD1):c.7575G>A (p.Leu2525=) rs371880816 0.00234
NM_144666.3(DNHD1):c.3736G>A (p.Ala1246Thr) rs186978440 0.00227
NM_144666.3(DNHD1):c.12770C>A (p.Pro4257His) rs138517528 0.00194
NM_144666.3(DNHD1):c.12931C>T (p.Arg4311Cys) rs200088426 0.00121
NM_144666.3(DNHD1):c.3612C>T (p.Gly1204=) rs376064043 0.00098
NM_144666.3(DNHD1):c.890A>G (p.Tyr297Cys) rs78466420 0.00066
NM_144666.3(DNHD1):c.1160G>A (p.Arg387Gln) rs147108806 0.00054
NM_144666.3(DNHD1):c.5904C>T (p.Ser1968=) rs149659254 0.00050
NM_144666.3(DNHD1):c.12728T>C (p.Ile4243Thr) rs184037935 0.00031
NM_144666.3(DNHD1):c.4072C>T (p.Arg1358Cys) rs12574381 0.00030
NM_144666.3(DNHD1):c.11979A>G (p.Leu3993=) rs143341167 0.00022
NM_144666.3(DNHD1):c.9936C>T (p.Asp3312=) rs369064736 0.00009
NM_144666.3(DNHD1):c.4908G>A (p.Ala1636=) rs200820770 0.00002
NM_144666.3(DNHD1):c.10329A>G (p.Leu3443=) rs556499381 0.00001
NM_144666.3(DNHD1):c.1848A>G (p.Glu616=) rs561432014
NM_144666.3(DNHD1):c.4041C>T (p.Ser1347=) rs189772244
NM_144666.3(DNHD1):c.5737_5738insATGCCCTACTGC (p.Leu1912_Arg1913insHisAlaLeuLeu) rs11268490

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.