Mutation

Primary Site >> Stomach Cancer

Gene >> AKAP6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32824730:32824730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529053250
CDS Mutation	c.6917T>G
AA Mutation	p.Leu2306Arg(p.L2306R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32545234:32545234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779406344
CDS Mutation	c.581G>A
AA Mutation	p.Arg194Gln(p.R194Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32822963:32822963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146242099
CDS Mutation	c.5150C>T
AA Mutation	p.Ser1717Leu(p.S1717L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32824557:32824557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6744G>T
AA Mutation	p.Lys2248Asn(p.K2248N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32546925:32546925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2272T>G
AA Mutation	p.Ser758Ala(p.S758A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32824648:32824648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6835G>T
AA Mutation	p.Asp2279Tyr(p.D2279Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32433631:32433631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.138G>A
AA Mutation	p.Met46Ile(p.M46I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32545329:32545329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>A
AA Mutation	p.Glu226Lys(p.E226K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32823760:32823760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5947T>C
AA Mutation	p.Ser1983Pro(p.S1983P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32824150:32824150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6337T>G
AA Mutation	p.Leu2113Val(p.L2113V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32822181:32822181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4368A>C
AA Mutation	p.Glu1456Asp(p.E1456D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32822978:32822978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5165T>C
AA Mutation	p.Leu1722Pro(p.L1722P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32822572:32822572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4759A>G
AA Mutation	p.Ser1587Gly(p.S1587G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32823758:32823758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5945A>C
AA Mutation	p.Lys1982Thr(p.K1982T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32546562:32546562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1909C>A
AA Mutation	p.Leu637Ile(p.L637I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32696004:32696004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2894A>T
AA Mutation	p.Asp965Val(p.D965V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32824726:32824726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6913A>C
AA Mutation	p.Asn2305His(p.N2305H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32822883:32822883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5070A>C
AA Mutation	p.Glu1690Asp(p.E1690D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32546494:32546494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1841T>C
AA Mutation	p.Val614Ala(p.V614A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32535797:32535797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568A>G
AA Mutation	p.Thr190Ala(p.T190A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32545897:32545897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1244T>C
AA Mutation	p.Val415Ala(p.V415A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000280979
Start	32824746:32824746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6933A>C
AA Mutation	p.Glu2311Asp(p.E2311D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280979
Start	32824149:32824149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6336C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280979
Start	32822340:32822340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4527C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280979
Start	32577233:32577233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2460G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280979
Start	32545919:32545919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1266C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280979
Start	32823666:32823666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5853A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280979
Start	32821560:32821560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3747G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280979
Start	32821599:32821599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749053344
CDS Mutation	c.3786C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280979
Start	32824146:32824146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762832602
CDS Mutation	c.6333G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280979
Start	32822754:32822754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4941G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280979
Start	32823966:32823966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760218256
CDS Mutation	c.6153C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280979
Start	32545823:32545823(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1174delA
AA Mutation	p.Arg392GlufsTer14(p.R392Efs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280979
Start	32823497:32823497(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5687delA
AA Mutation	p.Asn1896MetfsTer17(p.N1896Mfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280979
Start	32822329:32822329(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4521delA
AA Mutation	p.Lys1507AsnfsTer40(p.K1507Nfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280979
Start	32433625:32433625(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.133delG
AA Mutation	p.Asp45ThrfsTer35(p.D45Tfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000280979
Start	32735825:32735825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3315T>A
AA Mutation	p.Cys1105Ter(p.C1105*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000280979
Start	32546449:32546449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1796C>G
AA Mutation	p.Ser599Ter(p.S599*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000280979
Start	32822510:32822510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4697C>A
AA Mutation	p.Ser1566Ter(p.S1566*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280979
Start	32546098:32546099(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1448dupG
AA Mutation	p.Arg484LysfsTer3(p.R484Kfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	41
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000280979
Start	32821400:32821400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3589-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript