Mutation

Primary Site >> Stomach Cancer

Gene >> AKAP13

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85723083:85723083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764296768
CDS Mutation	c.6508G>C
AA Mutation	p.Glu2170Gln(p.E2170Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85579635:85579635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759395748
CDS Mutation	c.1567G>A
AA Mutation	p.Val523Ile(p.V523I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85723173:85723173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6598C>T
AA Mutation	p.Arg2200Cys(p.R2200C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85735605:85735605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371824645
CDS Mutation	c.7487C>T
AA Mutation	p.Thr2496Met(p.T2496M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85743640:85743640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8207G>T
AA Mutation	p.Arg2736Leu(p.R2736L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85485746:85485746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26C>T
AA Mutation	p.Pro9Leu(p.P9L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85645829:85645829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4249T>C
AA Mutation	p.Phe1417Leu(p.F1417L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85581278:85581278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3210G>T
AA Mutation	p.Lys1070Asn(p.K1070N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85580923:85580923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2855G>T
AA Mutation	p.Arg952Ile(p.R952I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85579365:85579365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1297C>T
AA Mutation	p.Pro433Ser(p.P433S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85533828:85533828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.426C>G
AA Mutation	p.His142Gln(p.H142Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85718028:85718028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5870A>G
AA Mutation	p.Glu1957Gly(p.E1957G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85578943:85578943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.875A>G
AA Mutation	p.Lys292Arg(p.K292R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85581748:85581748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3680C>G
AA Mutation	p.Thr1227Ser(p.T1227S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85719133:85719133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6059A>G
AA Mutation	p.Tyr2020Cys(p.Y2020C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85581364:85581364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3296G>T
AA Mutation	p.Gly1099Val(p.G1099V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85741182:85741182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7745A>G
AA Mutation	p.Gln2582Arg(p.Q2582R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85521519:85521519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142964345
CDS Mutation	c.125G>A
AA Mutation	p.Arg42His(p.R42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394518
Start	85734992:85734992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780717590
CDS Mutation	c.7283T>C
AA Mutation	p.Val2428Ala(p.V2428A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85741050:85741050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777033018
CDS Mutation	c.7613T>C
AA Mutation	p.Val2538Ala(p.V2538A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85682184:85682184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5128C>T
AA Mutation	p.His1710Tyr(p.H1710Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000394518
Start	85682164:85682164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5108G>A
AA Mutation	p.Arg1703Gln(p.R1703Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394518
Start	85581089:85581089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568102019
CDS Mutation	c.3021G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394518
Start	85741378:85741378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7941C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394518
Start	85730625:85730625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7200A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394518
Start	85581680:85581680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202239836
CDS Mutation	c.3612T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394518
Start	85727182:85727182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6939C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394518
Start	85735564:85735564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201887818
CDS Mutation	c.7446C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394518
Start	85735056:85735056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7347C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394518
Start	85581164:85581164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3096C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394518
Start	85655635:85655635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750404650
CDS Mutation	c.4593C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394518
Start	85580795:85580795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2727T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394518
Start	85735624:85735624(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7511delA
AA Mutation	p.Lys2504ArgfsTer50(p.K2504Rfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394518
Start	85581513:85581526(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3448_3461delCCAGAGATGATACC
AA Mutation	p.Pro1150SerfsTer2(p.P1150Sfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394518
Start	85579206:85579206(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1141delG
AA Mutation	p.Glu381LysfsTer29(p.E381Kfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394518
Start	85743786:85743786(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.8360delA
AA Mutation	p.Lys2787ArgfsTer34(p.K2787Rfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394518
Start	85719112:85719112(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6038delT
AA Mutation	p.Leu2013ProfsTer4(p.L2013Pfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394518
Start	85575235:85575236(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.770_771dupCT
AA Mutation	p.Glu258LeufsTer24(p.E258Lfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	39
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000394518
Start	85579374:85579375(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1306_1307insCTG
AA Mutation	p.Gln436delinsProGlu(p.Q436delinsPE)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript