Mutation

Primary Site >> Stomach Cancer

Gene >> ADCY10

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167809695:167809695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201892899
CDS Mutation	c.4816G>A
AA Mutation	p.Val1606Met(p.V1606M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367851
Start	167860872:167860872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772108925
CDS Mutation	c.1808A>G
AA Mutation	p.Gln603Arg(p.Q603R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167870276:167870276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1597G>T
AA Mutation	p.Ala533Ser(p.A533S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167870293:167870293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748513464
CDS Mutation	c.1580T>C
AA Mutation	p.Met527Thr(p.M527T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167878463:167878463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1389G>T
AA Mutation	p.Trp463Cys(p.W463C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167848415:167848415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2383C>T
AA Mutation	p.His795Tyr(p.H795Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167845999:167845999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2702C>T
AA Mutation	p.Pro901Leu(p.P901L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167883475:167883475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.982T>G
AA Mutation	p.Phe328Val(p.F328V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167901673:167901673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425G>A
AA Mutation	p.Arg142Gln(p.R142Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167854470:167854470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2191T>G
AA Mutation	p.Cys731Gly(p.C731G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167880504:167880504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1126G>T
AA Mutation	p.Val376Phe(p.V376F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167860938:167860938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377634034
CDS Mutation	c.1742G>A
AA Mutation	p.Arg581Gln(p.R581Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167856226:167856226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774828588
CDS Mutation	c.2110G>A
AA Mutation	p.Asp704Asn(p.D704N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167878482:167878482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1370G>T
AA Mutation	p.Gly457Val(p.G457V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167846018:167846018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779053477
CDS Mutation	c.2683C>T
AA Mutation	p.Arg895Cys(p.R895C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167836497:167836497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202210889
CDS Mutation	c.3121G>A
AA Mutation	p.Val1041Ile(p.V1041I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000367851
Start	167860893:167860893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1787T>A
AA Mutation	p.Leu596His(p.L596H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167845768:167845768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2802G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167823117:167823117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4059G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167824523:167824523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4005T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167854399:167854399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2262A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367851
Start	167893919:167893919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.762G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367851
Start	167896668:167896668(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.666delC
AA Mutation	p.Asn223IlefsTer27(p.N223Ifs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367851
Start	167901757:167901757(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.341delA
AA Mutation	p.Asn114ThrfsTer6(p.N114Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000367851
Start	167860954:167860954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531613788
CDS Mutation	c.1726C>T
AA Mutation	p.Arg576Ter(p.R576*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367851
Start	167878590:167878591(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1258_1261dupTACT
AA Mutation	p.Tyr421LeufsTer24(p.Y421Lfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367851
Start	167893927:167893928(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.752_753dupTT
AA Mutation	p.Ala252LeufsTer5(p.A252Lfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367851
Start	167809720:167809721(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs753500756
CDS Mutation	c.4790dupA
AA Mutation	p.Asn1597LysfsTer8(p.N1597Kfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	29
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000367851
Start	167875187:167875187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1407-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	30
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000367851
Start	167870279:167870302(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1571_1594delAGATACTTATGAAAATTGAGTACC
AA Mutation	p.Gln524_Tyr531del(p.Q524_Y531del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

ID	31
Mutation Consequence	start_lost
Transcription ID	ENST00000367851
Start	167905139:167905139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript