ClinVar Miner

List of variants reported as likely benign for respiratory system cancer by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (36):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_004562.3(PRKN):c.500G>A (p.Ser167Asn) rs1801474 0.05277
NM_004562.3(PRKN):c.1180G>A (p.Asp394Asn) rs1801334 0.02570
NM_000546.6(TP53):c.97-6C>T rs35117667 0.00847
NM_000124.4(ERCC6):c.3922G>C (p.Val1308Leu) rs2229761 0.00814
NM_004562.3(PRKN):c.136G>A (p.Ala46Thr) rs75860381 0.00621
NM_004562.3(PRKN):c.458C>G (p.Pro153Arg) rs55654276 0.00452
NM_005228.5(EGFR):c.3485G>A (p.Ser1162Asn) rs41321844 0.00362
NM_004333.6(BRAF):c.1141-19C>T rs71645959 0.00360
NM_001372051.1(CASP8):c.339C>T (p.Ser113=) rs17860422 0.00309
NM_002447.4(MST1R):c.1861A>T (p.Lys621Ter) rs9819888 0.00252
NM_177438.3(DICER1):c.1377-4T>G rs192490028 0.00240
NM_177438.3(DICER1):c.4891T>G (p.Ser1631Ala) rs145551486 0.00128
NM_177438.3(DICER1):c.1908-4A>G rs112284114 0.00123
NM_177438.3(DICER1):c.3213A>G (p.Arg1071=) rs148959399 0.00123
NM_177438.3(DICER1):c.5604-12G>A rs149841885 0.00122
NM_033360.4(KRAS):c.5-18A>G rs200189105 0.00100
NM_004333.6(BRAF):c.981-20C>T rs374896031 0.00066
NM_004333.6(BRAF):c.2127+3A>G rs371976102 0.00043
NM_000546.5(TP53):c.319T>C (p.Tyr107His) rs368771578 0.00028
NM_004985.5(KRAS):c.24A>G (p.Val8=) rs147406419 0.00025
NM_004333.6(BRAF):c.240+18A>G rs368584855 0.00017
NM_004333.6(BRAF):c.1860+16A>G rs368859030 0.00016
NM_000546.6(TP53):c.672+18G>C rs199578278 0.00014
NM_004562.3(PRKN):c.837C>T (p.His279=) rs149433924 0.00014
NM_033360.4(KRAS):c.90C>T (p.Asp30=) rs113623140 0.00011
NM_000546.6(TP53):c.847C>T (p.Arg283Cys) rs149633775 0.00009
NM_004333.6(BRAF):c.1993-11T>C rs750297886 0.00009
NM_004333.6(BRAF):c.399A>G (p.Ser133=) rs397507463 0.00009
NM_004333.6(BRAF):c.1694+13C>T rs368578780 0.00007
NM_004333.6(BRAF):c.504+19C>T rs780617193 0.00006
NM_033360.4(KRAS):c.4+5G>A rs201789109 0.00006
NM_004333.6(BRAF):c.915G>A (p.Ala305=) rs145675911 0.00004
NM_004562.3(PRKN):c.219G>A (p.Pro73=) rs139083077 0.00004
NM_004562.3(PRKN):c.276G>A (p.Ala92=) rs200256562 0.00004
NM_004985.5(KRAS):c.451-5652C>T rs727505314 0.00004
NM_004333.6(BRAF):c.1314+17T>C rs1057524397 0.00003
NM_004333.6(BRAF):c.2128-10_2128-9insC rs758588300 0.00003
NM_004333.6(BRAF):c.2136C>T (p.Ala712=) rs377165711 0.00003
NM_000546.6(TP53):c.-12C>T rs375229869 0.00002
NM_004333.6(BRAF):c.1433-18G>A rs763267814 0.00002
NM_000124.4(ERCC6):c.804A>G (p.Ala268=) rs777672678 0.00001
NM_004333.6(BRAF):c.1338G>A (p.Ser446=) rs765215499 0.00001
NM_004333.6(BRAF):c.1848C>A (p.Ser616=) rs752115982 0.00001
NM_004333.6(BRAF):c.1992+15C>T rs766089848 0.00001
NM_004333.6(BRAF):c.298T>C (p.Leu100=) rs761709697 0.00001
NM_004333.6(BRAF):c.712-18T>C rs535496777 0.00001
NM_177438.3(DICER1):c.1770T>C (p.Cys590=) rs777355058 0.00001
NM_177438.3(DICER1):c.3269+12C>T rs775380766 0.00001
NM_000321.3(RB1):c.485T>A (p.Phe162Tyr) rs764881599
NM_004333.6(BRAF):c.1206C>A (p.Pro402=) rs201758035
NM_004333.6(BRAF):c.1432+17_1432+19del rs777363183
NM_004333.6(BRAF):c.1719C>A (p.Ile573=) rs2128999629
NM_004333.6(BRAF):c.1992+16G>C rs3789806
NM_004333.6(BRAF):c.2128-27_2128-19del rs761539834
NM_004985.5(KRAS):c.112-9C>T rs727504298
NM_177438.3(DICER1):c.1510-4del rs546524688
NM_177438.3(DICER1):c.4608T>C (p.Gly1536=) rs1890331241

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