Mutation

Primary Site >> Stomach Cancer

Gene >> ABCB1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87566794:87566794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201280497
CDS Mutation	c.521G>A
AA Mutation	p.Arg174Gln(p.R174Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87531451:87531451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2528T>G
AA Mutation	p.Leu843Arg(p.L843R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87550006:87550006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1399C>T
AA Mutation	p.Arg467Trp(p.R467W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87519380:87519380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144369247
CDS Mutation	c.2873G>A
AA Mutation	p.Arg958Gln(p.R958Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87536504:87536504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2435G>A
AA Mutation	p.Gly812Glu(p.G812E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87515260:87515260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199943026
CDS Mutation	c.3253C>T
AA Mutation	p.Arg1085Trp(p.R1085W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87520873:87520873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147487745
CDS Mutation	c.2689G>A
AA Mutation	p.Ala897Thr(p.A897T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87549358:87549358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1715C>T
AA Mutation	p.Ala572Val(p.A572V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87544966:87544966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1921G>A
AA Mutation	p.Ala641Thr(p.A641T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87595788:87595788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95C>A
AA Mutation	p.Pro32Gln(p.P32Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87549925:87549925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1480A>G
AA Mutation	p.Asn494Asp(p.N494D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87549982:87549982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423C>A
AA Mutation	p.Gln475Lys(p.Q475K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87515292:87515292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3221G>T
AA Mutation	p.Cys1074Phe(p.C1074F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87519374:87519374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2879G>A
AA Mutation	p.Gly960Glu(p.G960E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87520843:87520843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573245329
CDS Mutation	c.2719G>A
AA Mutation	p.Val907Ile(p.V907I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87585610:87585610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188C>A
AA Mutation	p.Ala63Asp(p.A63D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87544843:87544843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2044C>T
AA Mutation	p.Leu682Phe(p.L682F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87531403:87531403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2576T>G
AA Mutation	p.Leu859Arg(p.L859R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87566176:87566176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596C>A
AA Mutation	p.Thr199Lys(p.T199K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87566883:87566883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432A>G
AA Mutation	p.Ile144Met(p.I144M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87545961:87545961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199931362
CDS Mutation	c.1789G>A
AA Mutation	p.Val597Ile(p.V597I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87553808:87553808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952A>G
AA Mutation	p.Thr318Ala(p.T318A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87544187:87544187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2153C>T
AA Mutation	p.Ala718Val(p.A718V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87566910:87566910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405T>G
AA Mutation	p.Phe135Leu(p.F135L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000265724
Start	87531334:87531334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2645A>G
AA Mutation	p.Gln882Arg(p.Q882R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265724
Start	87520844:87520844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2718C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265724
Start	87545950:87545950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1800T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265724
Start	87550555:87550555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200370991
CDS Mutation	c.1137G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265724
Start	87541450:87541450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2226T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265724
Start	87549896:87549896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1509T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265724
Start	87515252:87515252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200822574
CDS Mutation	c.3261C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265724
Start	87536513:87536513(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2426delA
AA Mutation	p.Asn809ThrfsTer6(p.N809Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265724
Start	87595784:87595787(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.96_99delAACT
AA Mutation	p.Thr33SerfsTer35(p.T33Sfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265724
Start	87544951:87544951(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1936delA
AA Mutation	p.Ser646ValfsTer17(p.S646Vfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265724
Start	87566170:87566170(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.602delT
AA Mutation	p.Phe201SerfsTer5(p.F201Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265724
Start	87516550:87516550(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3043delA
AA Mutation	p.Thr1015ProfsTer3(p.T1015Pfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000265724
Start	87519401:87519402(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2851_2852insCACAGTAGGG
AA Mutation	p.Phe951SerfsTer3(p.F951Sfs*3)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000265724
Start	87550039:87550039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1366C>T
AA Mutation	p.Gln456Ter(p.Q456*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000265724
Start	87531413:87531413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2566C>T
AA Mutation	p.Gln856Ter(p.Q856*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265724
Start	87550466:87550466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript