ClinVar Miner

List of variants in gene NDUFS2 reported as likely benign for not provided

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Gene type:
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Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_001377299.1(NDUFS2):c.1054C>G (p.Pro352Ala) rs11576415 0.06461
NM_001377299.1(NDUFS2):c.986+12A>G rs11265565 0.01793
NM_004550.5(NDUFS2):c.-239-201A>G rs115518404 0.01579
NM_001377299.1(NDUFS2):c.781-33G>A rs115682162 0.01455
NM_001377299.1(NDUFS2):c.95+243G>C rs114249790 0.01130
NM_001377299.1(NDUFS2):c.987-66C>T rs114007509 0.00659
NM_001377299.1(NDUFS2):c.514+11C>T rs76309459 0.00593
NM_001377299.1(NDUFS2):c.968G>A (p.Arg323Gln) rs35086265 0.00477
NM_001377299.1(NDUFS2):c.1117-187G>A rs77002109 0.00409
NM_001377299.1(NDUFS2):c.*108A>T rs191955041 0.00316
NM_001377299.1(NDUFS2):c.866+8G>A rs142594036 0.00231
NM_001377299.1(NDUFS2):c.627+3A>G rs111808262 0.00089
NM_001377299.1(NDUFS2):c.959T>C (p.Val320Ala) rs144937332 0.00081
NM_001377299.1(NDUFS2):c.628-12C>T rs202121443 0.00075
NM_001377299.1(NDUFS2):c.1138C>G (p.His380Asp) rs144411579 0.00055
NM_001377299.1(NDUFS2):c.1116+20A>G rs200063148 0.00044
NM_001377299.1(NDUFS2):c.1371A>G (p.Val457=) rs149953813 0.00040
NM_001377299.1(NDUFS2):c.117A>G (p.Pro39=) rs145578059 0.00019
NM_001377299.1(NDUFS2):c.1354+10C>A rs201275792 0.00018
NM_001377299.1(NDUFS2):c.600C>T (p.Phe200=) rs138185030 0.00017
NM_001377299.1(NDUFS2):c.393+12G>A rs180970484 0.00011
NM_001377299.1(NDUFS2):c.1213-20C>T rs139327184 0.00009
NM_001377299.1(NDUFS2):c.285G>A (p.Leu95=) rs764795771 0.00009
NM_001377299.1(NDUFS2):c.273G>A (p.Ala91=) rs370126952 0.00008
NM_001377299.1(NDUFS2):c.339C>T (p.Ile113=) rs374883390 0.00007
NM_001377299.1(NDUFS2):c.628-11G>A rs370433084 0.00007
NM_001377299.1(NDUFS2):c.1355-7C>T rs749095282 0.00005
NM_001377299.1(NDUFS2):c.1278T>C (p.Ala426=) rs746338268 0.00004
NM_001377299.1(NDUFS2):c.96-8C>T rs748230530 0.00004
NM_001377299.1(NDUFS2):c.177C>T (p.Ala59=) rs755626092 0.00003
NM_001377299.1(NDUFS2):c.777G>A (p.Glu259=) rs763804955 0.00003
NM_001377299.1(NDUFS2):c.1324C>T (p.His442Tyr) rs201897431 0.00002
NM_001377299.1(NDUFS2):c.203-8C>T rs750025366 0.00002
NM_001377299.1(NDUFS2):c.354A>G (p.Arg118=) rs1218305354 0.00002
NM_001377299.1(NDUFS2):c.394-8C>T rs770508509 0.00001
NM_001377299.1(NDUFS2):c.515-10G>A rs1292747569 0.00001
NM_001377299.1(NDUFS2):c.*78GT[20] rs10629771
NM_001377299.1(NDUFS2):c.*78GT[21] rs10629771
NM_001377299.1(NDUFS2):c.1089G>T (p.Val363=)
NM_001377299.1(NDUFS2):c.1117-15G>A rs1296999118
NM_001377299.1(NDUFS2):c.114G>A (p.Gln38=) rs2102030615
NM_001377299.1(NDUFS2):c.1212+13G>A
NM_001377299.1(NDUFS2):c.1213-6G>A
NM_001377299.1(NDUFS2):c.1213-9del rs750838845
NM_001377299.1(NDUFS2):c.1354+18T>C rs372304828
NM_001377299.1(NDUFS2):c.150T>A (p.Ala50=)
NM_001377299.1(NDUFS2):c.186G>A (p.Lys62=)
NM_001377299.1(NDUFS2):c.203-8C>A
NM_001377299.1(NDUFS2):c.267A>G (p.Pro89=)
NM_001377299.1(NDUFS2):c.394-18A>G
NM_001377299.1(NDUFS2):c.472T>C (p.Leu158=)
NM_001377299.1(NDUFS2):c.492T>G (p.Pro164=)
NM_001377299.1(NDUFS2):c.514+19_514+20dup
NM_001377299.1(NDUFS2):c.515-20T>C
NM_001377299.1(NDUFS2):c.517C>T (p.Leu173=) rs1571614920
NM_001377299.1(NDUFS2):c.519G>A (p.Leu173=)
NM_001377299.1(NDUFS2):c.567A>G (p.Thr189=)
NM_001377299.1(NDUFS2):c.627+18G>C
NM_001377299.1(NDUFS2):c.628-17del rs775653766
NM_001377299.1(NDUFS2):c.628-8C>T
NM_001377299.1(NDUFS2):c.646C>A (p.Arg216=)
NM_001377299.1(NDUFS2):c.660C>T (p.Ala220=)
NM_001377299.1(NDUFS2):c.672T>C (p.Ala224=)
NM_001377299.1(NDUFS2):c.702+20C>G
NM_001377299.1(NDUFS2):c.703-13G>A
NM_001377299.1(NDUFS2):c.780+16A>G
NM_001377299.1(NDUFS2):c.781-16T>C
NM_001377299.1(NDUFS2):c.813G>T (p.Arg271=)
NM_001377299.1(NDUFS2):c.816A>G (p.Thr272=) rs755330962
NM_001377299.1(NDUFS2):c.918G>A (p.Gln306=) rs2102049365
NM_001377299.1(NDUFS2):c.942T>C (p.Val314=) rs1571617771
NM_001377299.1(NDUFS2):c.969A>G (p.Arg323=)
NM_001377299.1(NDUFS2):c.987-273G>C rs74469233

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