Mutation

Primary Site >> Stomach Cancer

Gene >> ADCY3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24918443:24918443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545C>T
AA Mutation	p.Thr182Met(p.T182M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24828029:24828029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2305G>A
AA Mutation	p.Val769Met(p.V769M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260600
Start	24838620:24838620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777689844
CDS Mutation	c.1358G>A
AA Mutation	p.Arg453His(p.R453H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24837000:24837000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579G>A
AA Mutation	p.Ala527Thr(p.A527T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24824476:24824476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369517755
CDS Mutation	c.2638C>T
AA Mutation	p.Arg880Cys(p.R880C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24828058:24828058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2276T>C
AA Mutation	p.Val759Ala(p.V759A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24834506:24834506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1946T>C
AA Mutation	p.Val649Ala(p.V649A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24918663:24918663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.325G>A
AA Mutation	p.Ala109Thr(p.A109T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24830782:24830782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150335965
CDS Mutation	c.2099G>A
AA Mutation	p.Arg700Gln(p.R700Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24840012:24840012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1216A>G
AA Mutation	p.Lys406Glu(p.K406E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24821523:24821523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3121C>T
AA Mutation	p.Arg1041Cys(p.R1041C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24834927:24834927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1672C>T
AA Mutation	p.Pro558Ser(p.P558S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000260600
Start	24834599:24834599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1853C>T
AA Mutation	p.Pro618Leu(p.P618L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24820079:24820079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762117912
CDS Mutation	c.3288C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24820835:24820835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556248650
CDS Mutation	c.3141C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24918661:24918661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147964025
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24918682:24918682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24918910:24918910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260600
Start	24841595:24841595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1029G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260600
Start	24918608:24918608(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.380delA
AA Mutation	p.Lys127ArgfsTer21(p.K127Rfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260600
Start	24839985:24839985(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1243delG
AA Mutation	p.Val415CysfsTer27(p.V415Cfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260600
Start	24839960:24839960(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1268delG
AA Mutation	p.Gly423AlafsTer19(p.G423Afs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000260600
Start	24824461:24824461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2653C>T
AA Mutation	p.Arg885Ter(p.R885*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260600
Start	24822546:24822547(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2967dupC
AA Mutation	p.Asp990ArgfsTer26(p.D990Rfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript