NM_005228.5(EGFR):c.2369C>T (p.Thr790Met)
|
rs121434569
|
0.00005
|
NM_005228.5(EGFR):c.2326C>T (p.Arg776Cys)
|
rs1275022697
|
0.00001
|
NM_000546.6(TP53):c.314G>T (p.Gly105Val)
|
rs587781504
|
|
NM_004333.6(BRAF):c.1742A>G (p.Asn581Ser)
|
rs121913370
|
|
NM_004333.6(BRAF):c.1780G>A (p.Asp594Asn)
|
rs397516896
|
|
NM_004333.6(BRAF):c.1781A>G (p.Asp594Gly)
|
rs121913338
|
|
NM_004333.6(BRAF):c.1801A>G (p.Lys601Glu)
|
rs121913364
|
|
NM_004448.4(ERBB2):c.2263_2264delinsCC (p.Leu755Pro)
|
rs121913469
|
|
NM_004448.4(ERBB2):c.2313_2324dup (p.Tyr772_Ala775dup)
|
rs397516975
|
|
NM_004448.4(ERBB2):c.2314_2325dup (p.Tyr772_Ala775dup)
|
rs397516977
|
|
NM_004448.4(ERBB2):c.2331_2339dup (p.Gly778_Pro780dup)
|
rs397516981
|
|
NM_004562.3(PRKN):c.601_602insA (p.Cys201Ter)
|
rs1231455463
|
|
NM_005228.5(EGFR):c.2126A>C (p.Glu709Ala)
|
rs397517085
|
|
NM_005228.5(EGFR):c.2155G>A (p.Gly719Ser)
|
rs28929495
|
|
NM_005228.5(EGFR):c.2235_2249del (p.Glu746_Ala750del)
|
rs121913421
|
|
NM_005228.5(EGFR):c.2236_2250del (p.Glu746_Ala750del)
|
rs727504233
|
|
NM_005228.5(EGFR):c.2237_2255delinsT (p.Glu746_Ser752delinsVal)
|
rs727504258
|
|
NM_005228.5(EGFR):c.2239_2248delinsC (p.Leu747_Ala750delinsPro)
|
rs727504278
|
|
NM_005228.5(EGFR):c.2239_2256del (p.Leu747_Ser752del)
|
rs121913440
|
|
NM_005228.5(EGFR):c.2239_2256delinsCAA (p.Leu747_Ser752delinsGln)
|
rs2128954790
|
|
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.2252_2277delinsAT (p.Thr751_Ile759delinsAsn)
|
rs397517100
|
|
NM_005228.5(EGFR):c.2303_2311dup (p.Ser768_Asp770dup)
|
rs397517109
|
|
NM_005228.5(EGFR):c.2309_2310insGTC (p.Asp770delinsGluSer)
|
rs1554350382
|
|
NM_005228.5(EGFR):c.2318_2320delinsTCA (p.His773_Val774delinsLeuMet)
|
rs2534769494
|
|
NM_005228.5(EGFR):c.2497T>G (p.Leu833Val)
|
rs397517126
|
|
NM_005228.5(EGFR):c.2499G>T (p.Leu833Phe)
|
rs2128964427
|
|
NM_005228.5(EGFR):c.2500G>T (p.Val834Leu)
|
rs397517127
|
|
NM_005228.5(EGFR):c.2504A>T (p.His835Leu)
|
rs397517128
|
|
NM_005228.5(EGFR):c.2555A>C (p.Lys852Thr)
|
rs1292517709
|
|
NM_005228.5(EGFR):c.2573T>G (p.Leu858Arg)
|
rs121434568
|
|
NM_005228.5(EGFR):c.2582T>A (p.Leu861Gln)
|
rs121913444
|
|
NM_005228.5(EGFR):c.709_710delinsTT (p.Ala237Phe)
|
rs2535499036
|
|
NM_016507.4(CDK12):c.2636G>T (p.Gly879Val)
|
rs1131692238
|
|
t(8;10)(q12.1;q23.31)
|
|
|