ClinVar Miner

List of variants reported as drug response by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 58
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HGVS dbSNP
NM_000771.3(CYP2C9):c.[430C=;1075A=]
NM_000771.3(CYP2C9):c.[430C=;1075A>C]
NM_000771.3(CYP2C9):c.[430C>T;1075A=]
NM_005228.5(EGFR):c.2125G>A (p.Glu709Lys) rs727504256
NM_005228.5(EGFR):c.2126A>G (p.Glu709Gly) rs397517085
NM_005228.5(EGFR):c.2155G>A (p.Gly719Ser) rs28929495
NM_005228.5(EGFR):c.2230_2249delinsGTCAA (p.Ile744_Ala750delinsValLys) rs727503014
NM_005228.5(EGFR):c.2231_2232insAAAATTCCCGTCGCTA (p.Glu746fs) rs727504326
NM_005228.5(EGFR):c.2232_2250del (p.Lys745fs) rs727504324
NM_005228.5(EGFR):c.2232_2252delinsAAAGTT (p.Glu746_Thr751delinsLeu) rs727504428
NM_005228.5(EGFR):c.2235_2243del (p.Leu747_Glu749del) rs727504266
NM_005228.5(EGFR):c.2235_2248delinsAATTC (p.Glu746_Ala750delinsIlePro) rs727504281
NM_005228.5(EGFR):c.2235_2249del (p.Glu746_Ala750del) rs121913421
NM_005228.5(EGFR):c.2235_2251delinsAATTC (p.Glu746_Thr751delinsIlePro) rs727504332
NM_005228.5(EGFR):c.2236_2250del (p.Glu746_Ala750del) rs727504233
NM_005228.5(EGFR):c.2236_2252delinsAT (p.Glu746_Thr751delinsIle) rs727504402
NM_005228.5(EGFR):c.2237_2246delinsC (p.Glu746_Glu749delinsAla) rs727504444
NM_005228.5(EGFR):c.2237_2248delinsCAC (p.Glu746_Ala750delinsAlaPro) rs727503015
NM_005228.5(EGFR):c.2237_2248delinsCCC (p.Glu746_Ala750delinsAlaPro) rs727503015
NM_005228.5(EGFR):c.2237_2251del (p.Glu746_Thr751delinsAla) rs121913425
NM_005228.5(EGFR):c.2237_2251delinsTTC (p.Glu746_Thr751delinsValPro) rs727503016
NM_005228.5(EGFR):c.2237_2254del (p.Glu746_Ser752delinsAla) rs121913422
NM_005228.5(EGFR):c.2237_2255delinsT (p.Glu746_Ser752delinsVal) rs727504258
NM_005228.5(EGFR):c.2237_2256delinsTC (p.Glu746_Ser752delinsVal) rs121913424
NM_005228.5(EGFR):c.2237_2257delinsTCT (p.Glu746_Pro753delinsValSer) rs727504282
NM_005228.5(EGFR):c.2238_2248delinsGC (p.Leu747_Ala750delinsPro) rs121913435
NM_005228.5(EGFR):c.2238_2251delinsGC (p.Leu747_Thr751delinsPro) rs727504257
NM_005228.5(EGFR):c.2239_2247del (p.Leu747_Glu749del) rs121913436
NM_005228.5(EGFR):c.2239_2248delinsC (p.Leu747_Ala750delinsPro) rs727504278
NM_005228.5(EGFR):c.2239_2251delinsC (p.Leu747_Thr751delinsPro) rs397509368
NM_005228.5(EGFR):c.2239_2256del (p.Leu747_Ser752del) rs121913440
NM_005228.5(EGFR):c.2239_2257delinsA (p.Leu747_Pro753delinsThr) rs727504339
NM_005228.5(EGFR):c.2239_2257delinsCAAT (p.Leu747_Pro753delinsGlnSer) rs727504339
NM_005228.5(EGFR):c.2239_2264delinsACGAGAGA (p.Leu747_Ala755delinsThrArgAsp) rs727504414
NM_005228.5(EGFR):c.2240_2254del (p.Leu747_Thr751del) rs121913442
NM_005228.5(EGFR):c.2240_2257del (p.Leu747_Pro753delinsSer) rs121913438
NM_005228.5(EGFR):c.2251_2277delinsGAT (p.Thr751_Ile759delinsAsp) rs727504395
NM_005228.5(EGFR):c.2252C>T (p.Thr751Ile) rs727504316
NM_005228.5(EGFR):c.2253_2276del (p.Ser752_Ile759del) rs727504232
NM_005228.5(EGFR):c.2254_2277del (p.Ser752_Ile759del) rs121913463
NM_005228.5(EGFR):c.2292_2293insCATCAC (p.Val765_Met766insHisHis) rs1554350337
NM_005228.5(EGFR):c.2300_2308dup (p.Ala767_Val769dup) rs727504263
NM_005228.5(EGFR):c.2303_2311dup (p.Ser768_Asp770dup) rs397517109
NM_005228.5(EGFR):c.2307_2315dup (p.Asp770_Pro772dup) rs730880333
NM_005228.5(EGFR):c.2308_2309insGTT (p.Asp770delinsGlyTyr) rs1554350347
NM_005228.5(EGFR):c.2308_2310delinsTGGG (p.Asp770fs) rs727503019
NM_005228.5(EGFR):c.2308_2322dup (p.Asp770_Val774dup) rs1554350367
NM_005228.5(EGFR):c.2311A>G (p.Asn771Asp) rs727503020
NM_005228.5(EGFR):c.2311_2312insCAC (p.Asn771delinsThrHis) rs1554350351
NM_005228.5(EGFR):c.2311_2312insGTT (p.Asn771delinsSerTyr) rs1554350351
NM_005228.5(EGFR):c.2311_2319dup (p.Asn771_His773dup) rs397517115
NM_005228.5(EGFR):c.2312_2313insTGT (p.Pro772_His773insVal) rs727503021
NM_005228.5(EGFR):c.2317_2318insCGAACCCCC (p.His773_Val774insProAsnPro) rs727503013
NM_005228.5(EGFR):c.2369C>T (p.Thr790Met) rs121434569
NM_005228.5(EGFR):c.2573T>G (p.Leu858Arg) rs121434568
NM_005228.5(EGFR):c.2582T>A (p.Leu861Gln) rs121913444
NM_024006.4(VKORC1):c.-1639G>A rs9923231
NM_024006.5(VKORC1):c.-226-1413G= rs9923231

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