NM_005105.5(RBM8A):c.-21G>A
|
rs139428292
|
0.01871
|
NM_032043.3(BRIP1):c.2392C>T (p.Arg798Ter)
|
rs137852986
|
0.00010
|
NM_000136.3(FANCC):c.1642C>T (p.Arg548Ter)
|
rs104886457
|
0.00007
|
NM_000059.4(BRCA2):c.4965C>G (p.Tyr1655Ter)
|
rs80358721
|
0.00004
|
NM_001018115.3(FANCD2):c.2605+1G>A
|
rs142365855
|
0.00003
|
NM_001113378.2(FANCI):c.2422A>T (p.Lys808Ter)
|
rs375656231
|
0.00001
|
NM_005199.5(CHRNG):c.136C>T (p.Arg46Ter)
|
rs121912672
|
0.00001
|
NM_000059.4(BRCA2):c.5350_5351del (p.Asn1784fs)
|
rs80359507
|
|
NM_000059.4(BRCA2):c.7007G>C (p.Arg2336Pro)
|
rs28897743
|
|
NM_001374353.1(GLI2):c.3523C>T (p.Gln1175Ter)
|
|
|
NM_001378183.1(PIEZO2):c.8386A>G (p.Lys2796Glu)
|
rs2033787153
|
|
NM_001429.4(EP300):c.2225del (p.Pro742fs)
|
rs2059021664
|
|
NM_001429.4(EP300):c.2660C>T (p.Thr887Ile)
|
rs953108559
|
|
NM_001429.4(EP300):c.3592T>C (p.Tyr1198His)
|
rs1305375514
|
|
NM_002334.4(LRP4):c.5168A>G (p.His1723Arg)
|
|
|
NM_002334.4(LRP4):c.694C>A (p.Arg232Ser)
|
|
|
NM_002875.5(RAD51):c.772G>A (p.Glu258Lys)
|
rs1555429629
|
|
NM_002968.3(SALL1):c.721A>G (p.Ile241Val)
|
rs2143449563
|
|
NM_002968.3(SALL1):c.826C>T (p.Arg276Ter)
|
rs104894537
|
|
NM_004247.4(EFTUD2):c.2199G>A (p.Trp733Ter)
|
rs2145438293
|
|
NM_004247.4(EFTUD2):c.593dup (p.Tyr198Ter)
|
|
|
NM_004380.3(CREBBP):c.2436_2437insGCTG (p.Pro813fs)
|
rs2141214738
|
|
NM_004380.3(CREBBP):c.3779+1G>A
|
rs587783483
|
|
NM_004380.3(CREBBP):c.5790dup (p.Thr1931fs)
|
rs1596786512
|
|
NM_004380.3(CREBBP):c.5991del (p.Pro1997_Val1998insTer)
|
|
|
NM_006296.7(VRK2):c.*102_*105dup
|
rs759217526
|
|
NM_006306.4(SMC1A):c.1114-2A>G
|
rs1569358628
|
|
NM_006306.4(SMC1A):c.1829A>G (p.Gln610Arg)
|
|
|
NM_006306.4(SMC1A):c.3039G>C (p.Gln1013His)
|
|
|
NM_016653.3(MAP3K20):c.1592C>A (p.Ser531Ter)
|
rs3769148
|
|
NM_020436.5(SALL4):c.1068del (p.Lys357fs)
|
rs2122964551
|
|
NM_020928.2(ZSWIM6):c.3487C>T (p.Arg1163Trp)
|
rs587777695
|
|
NM_133433.4(NIPBL):c.1849G>A (p.Glu617Lys)
|
rs1744586399
|
|
NM_133433.4(NIPBL):c.6527T>C (p.Leu2176Pro)
|
rs1561207924
|
|
NM_152274.5(CCNQ):c.651G>A (p.Trp217Ter)
|
rs2148299424
|
|
NM_181486.4(TBX5):c.454C>G (p.Leu152Val)
|
rs2136416738
|
|