Mutation

Primary Site >> Stomach Cancer

Gene >> ATM

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108331930:108331930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7681C>A
AA Mutation	p.Leu2561Met(p.L2561M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108244096:108244096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747053710
CDS Mutation	c.640T>C
AA Mutation	p.Ser214Pro(p.S214P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108330378:108330378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7472G>T
AA Mutation	p.Trp2491Leu(p.W2491L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108289748:108289748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4383G>T
AA Mutation	p.Trp1461Cys(p.W1461C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000278616
Start	108272851:108272851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3283A>G
AA Mutation	p.Arg1095Gly(p.R1095G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108330350:108330350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7444A>G
AA Mutation	p.Met2482Val(p.M2482V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108289762:108289762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749770110
CDS Mutation	c.4397G>A
AA Mutation	p.Arg1466Gln(p.R1466Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108227692:108227692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587779858
CDS Mutation	c.68G>A
AA Mutation	p.Arg23Gln(p.R23Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108267315:108267315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2611G>A
AA Mutation	p.Glu871Lys(p.E871K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108281160:108281160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3568G>C
AA Mutation	p.Val1190Leu(p.V1190L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108317444:108317444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6270C>A
AA Mutation	p.Asp2090Glu(p.D2090E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108329124:108329124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7193A>G
AA Mutation	p.Tyr2398Cys(p.Y2398C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108329159:108329159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193302874
CDS Mutation	c.7228T>C
AA Mutation	p.Phe2410Leu(p.F2410L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108247071:108247071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138398778
CDS Mutation	c.1009C>T
AA Mutation	p.Arg337Cys(p.R337C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108347362:108347362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587779874
CDS Mutation	c.8668C>G
AA Mutation	p.Leu2890Val(p.L2890V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108272574:108272574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3120G>A
AA Mutation	p.Met1040Ile(p.M1040I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108335080:108335080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587782719
CDS Mutation	c.8122G>A
AA Mutation	p.Asp2708Asn(p.D2708N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108250979:108250979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1514T>G
AA Mutation	p.Phe505Cys(p.F505C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108345818:108345818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587779872
CDS Mutation	c.8494C>T
AA Mutation	p.Arg2832Cys(p.R2832C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108244856:108244856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.731C>T
AA Mutation	p.Ala244Val(p.A244V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108227689:108227689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.65A>G
AA Mutation	p.Glu22Gly(p.E22G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108304823:108304823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587782236
CDS Mutation	c.5645G>A
AA Mutation	p.Arg1882Gln(p.R1882Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108297354:108297354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4977A>G
AA Mutation	p.Ile1659Met(p.I1659M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108335015:108335015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8057T>G
AA Mutation	p.Phe2686Cys(p.F2686C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108289089:108289089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4222C>T
AA Mutation	p.Leu1408Phe(p.L1408F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108331949:108331949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7700A>G
AA Mutation	p.Asn2567Ser(p.N2567S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108365359:108365359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587782292
CDS Mutation	c.9022C>T
AA Mutation	p.Arg3008Cys(p.R3008C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108343322:108343322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8369G>A
AA Mutation	p.Arg2790Lys(p.R2790K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000278616
Start	108247066:108247066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004G>A
AA Mutation	p.Gly335Glu(p.G335E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278616
Start	108259057:108259057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2448A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278616
Start	108299727:108299727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5019C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278616
Start	108284434:108284434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3954C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278616
Start	108325469:108325469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6732A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278616
Start	108284386:108284386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3906T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278616
Start	108227636:108227636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs786201365
CDS Mutation	c.12A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278616
Start	108257498:108257498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2268A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278616
Start	108304812:108304812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767070325
CDS Mutation	c.5634G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278616
Start	108247047:108247051(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.986_990delGAGGA
AA Mutation	p.Arg329LysfsTer8(p.R329Kfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278616
Start	108289070:108289070(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4207delA
AA Mutation	p.Ser1403AlafsTer3(p.S1403Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278616
Start	108307929:108307929(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5712delA
AA Mutation	p.Lys1904AsnfsTer13(p.K1904Nfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278616
Start	108345750:108345750(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759472682
CDS Mutation	c.8432delA
AA Mutation	p.Lys2811SerfsTer46(p.K2811Sfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278616
Start	108244090:108244090(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.640delT
AA Mutation	p.Ser214ProfsTer16(p.S214Pfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278616
Start	108345750:108345751(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.8431_8432delAA
AA Mutation	p.Lys2811ValfsTer3(p.K2811Vfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278616
Start	108289059:108289059(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4195delA
AA Mutation	p.Thr1399ProfsTer3(p.T1399Pfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278616
Start	108289724:108289724(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4363delA
AA Mutation	p.Ser1455ValfsTer3(p.S1455Vfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	46
Mutation Consequence	stop_gained
Transcription ID	ENST00000278616
Start	108292680:108292680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4498C>T
AA Mutation	p.Gln1500Ter(p.Q1500*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	47
Mutation Consequence	stop_gained
Transcription ID	ENST00000278616
Start	108332765:108332765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138941496
CDS Mutation	c.7792C>T
AA Mutation	p.Arg2598Ter(p.R2598*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	48
Mutation Consequence	stop_gained
Transcription ID	ENST00000278616
Start	108343240:108343240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8287C>T
AA Mutation	p.Arg2763Ter(p.R2763*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	49
Mutation Consequence	stop_gained
Transcription ID	ENST00000278616
Start	108365142:108365142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8911C>T
AA Mutation	p.Gln2971Ter(p.Q2971*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	50
Mutation Consequence	stop_gained
Transcription ID	ENST00000278616
Start	108250960:108250960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1495C>T
AA Mutation	p.Gln499Ter(p.Q499*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	51
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278616
Start	108247085:108247086(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1026dupA
AA Mutation	p.Glu343ArgfsTer5(p.E343Rfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	52
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278616
Start	108301698:108301699(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5231dupA
AA Mutation	p.Thr1745AspfsTer4(p.T1745Dfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278616
Start	108293436:108293437(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.4741dupA
AA Mutation	p.Ile1581AsnfsTer5(p.I1581Nfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	54
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000278616
Start	108321300:108321300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6453-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript