Mutation

Primary Site >> Stomach Cancer

Gene >> ATAD2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123347343:123347343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1961G>A
AA Mutation	p.Arg654His(p.R654H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123369960:123369960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149848860
CDS Mutation	c.792T>A
AA Mutation	p.Asp264Glu(p.D264E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123322969:123322969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147449805
CDS Mutation	c.4100G>A
AA Mutation	p.Arg1367His(p.R1367H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123339394:123339394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2771C>T
AA Mutation	p.Pro924Leu(p.P924L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123333930:123333930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3426G>C
AA Mutation	p.Glu1142Asp(p.E1142D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123347206:123347206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2098G>A
AA Mutation	p.Ala700Thr(p.A700T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123328480:123328480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756836955
CDS Mutation	c.3578C>T
AA Mutation	p.Ala1193Val(p.A1193V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123369166:123369166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941A>G
AA Mutation	p.His314Arg(p.H314R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123322975:123322975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111422836
CDS Mutation	c.4094G>A
AA Mutation	p.Arg1365Gln(p.R1365Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123359270:123359270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1333C>T
AA Mutation	p.Pro445Ser(p.P445S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123371742:123371742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749840287
CDS Mutation	c.464G>A
AA Mutation	p.Arg155His(p.R155H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123359306:123359306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200411614
CDS Mutation	c.1297A>G
AA Mutation	p.Asn433Asp(p.N433D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123346183:123346183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2435C>A
AA Mutation	p.Ala812Asp(p.A812D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123359237:123359237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1366A>G
AA Mutation	p.Lys456Glu(p.K456E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123371244:123371244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631A>C
AA Mutation	p.Thr211Pro(p.T211P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123334319:123334319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3215G>A
AA Mutation	p.Arg1072His(p.R1072H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000287394
Start	123328315:123328315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3743T>C
AA Mutation	p.Ile1248Thr(p.I1248T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287394
Start	123325977:123325977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3918G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287394
Start	123349362:123349362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1729C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287394
Start	123344992:123344992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2610A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287394
Start	123336503:123336503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3081A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287394
Start	123325974:123325974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3921G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287394
Start	123323039:123323039(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4030delA
AA Mutation	p.Ser1344ValfsTer15(p.S1344Vfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287394
Start	123328522:123328522(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3536delA
AA Mutation	p.Lys1179SerfsTer16(p.K1179Sfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287394
Start	123359642:123359642(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1201delT
AA Mutation	p.Tyr401IlefsTer5(p.Y401Ifs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000287394
Start	123349338:123349338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1753C>T
AA Mutation	p.Arg585Ter(p.R585*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000287394
Start	123323045:123323045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4024A>T
AA Mutation	p.Lys1342Ter(p.K1342*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000287394
Start	123361645:123361645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1051C>T
AA Mutation	p.Arg351Ter(p.R351*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000287394
Start	123359287:123359292(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1311_1316delTCTAAA
AA Mutation	p.Leu438_Lys439del(p.L438_K439del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript