Mutation

Primary Site >> Stomach Cancer

Gene >> TRIP12

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229807778:229807778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373429636
CDS Mutation	c.2282C>T
AA Mutation	p.Ala761Val(p.A761V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229859239:229859239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434G>A
AA Mutation	p.Arg145Gln(p.R145Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229789664:229789664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4417C>A
AA Mutation	p.Leu1473Ile(p.L1473I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229810942:229810942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2015T>C
AA Mutation	p.Val672Ala(p.V672A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229774129:229774129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5437G>A
AA Mutation	p.Val1813Ile(p.V1813I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229858837:229858837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836T>C
AA Mutation	p.Leu279Pro(p.L279P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229799356:229799356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3009A>T
AA Mutation	p.Lys1003Asn(p.K1003N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229808302:229808302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2145T>A
AA Mutation	p.Asp715Glu(p.D715E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229807764:229807764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777391885
CDS Mutation	c.2296C>T
AA Mutation	p.Arg766Cys(p.R766C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229789682:229789682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4399C>T
AA Mutation	p.Pro1467Ser(p.P1467S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229818471:229818471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348G>A
AA Mutation	p.Asp450Asn(p.D450N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229785842:229785842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4784G>A
AA Mutation	p.Arg1595Gln(p.R1595Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000283943
Start	229778479:229778479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5093G>A
AA Mutation	p.Arg1698His(p.R1698H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283943
Start	229769263:229769263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5646C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283943
Start	229804169:229804169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371540901
CDS Mutation	c.2484G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283943
Start	229768695:229768695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5703G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283943
Start	229804094:229804094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753225320
CDS Mutation	c.2559G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283943
Start	229769272:229769272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5637G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283943
Start	229808323:229808323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2124A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283943
Start	229815106:229815107(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1579_1580delTT
AA Mutation	p.Leu527ArgfsTer10(p.L527Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000283943
Start	229787505:229787505(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4770delA
AA Mutation	p.Lys1590AsnfsTer4(p.K1590Nfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283943
Start	229791144:229791144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4298delA
AA Mutation	p.Lys1433SerfsTer18(p.K1433Sfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283943
Start	229807828:229807828(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2232delT
AA Mutation	p.Phe744LeufsTer7(p.F744Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000283943
Start	229791128:229791128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4314G>A
AA Mutation	p.Trp1438Ter(p.W1438*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000283943
Start	229799355:229799355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3010C>T
AA Mutation	p.Arg1004Ter(p.R1004*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283943
Start	229859399:229859400(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.273dupA
AA Mutation	p.Pro92ThrfsTer8(p.P92Tfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000283943
Start	229813868:229813868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1842+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript