Mutation

Primary Site >> Stomach Cancer

Gene >> ZC3H12A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37480334:37480334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488C>T
AA Mutation	p.Ala163Val(p.A163V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37481754:37481754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.737A>G
AA Mutation	p.Tyr246Cys(p.Y246C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37475504:37475504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8G>A
AA Mutation	p.Gly3Asp(p.G3D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37482979:37482979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1168C>T
AA Mutation	p.Arg390Cys(p.R390C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37483521:37483521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1710G>T
AA Mutation	p.Glu570Asp(p.E570D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37475828:37475828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332G>A
AA Mutation	p.Arg111Gln(p.R111Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37481658:37481658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641G>A
AA Mutation	p.Arg214Gln(p.R214Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37481634:37481634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201388317
CDS Mutation	c.617A>T
AA Mutation	p.Lys206Met(p.K206M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37483568:37483568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1757C>T
AA Mutation	p.Ala586Val(p.A586V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37483112:37483112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301A>T
AA Mutation	p.Asp434Val(p.D434V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37482877:37482877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373138865
CDS Mutation	c.1066C>T
AA Mutation	p.Arg356Trp(p.R356W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37483255:37483255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773544941
CDS Mutation	c.1444G>A
AA Mutation	p.Ala482Thr(p.A482T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37483446:37483446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635G>T
AA Mutation	p.Arg545Ser(p.R545S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373087
Start	37481662:37481662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373087
Start	37483125:37483125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1314G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373087
Start	37483125:37483125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746044726
CDS Mutation	c.1314G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373087
Start	37483341:37483341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1530A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373087
Start	37483014:37483014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748027131
CDS Mutation	c.1203A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373087
Start	37482954:37482954(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1147delG
AA Mutation	p.Ala383ProfsTer12(p.A383Pfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373087
Start	37482844:37482844(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1038delC
AA Mutation	p.Arg347GlufsTer22(p.R347Efs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373087
Start	37480376:37480379(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.533_536delTTGT
AA Mutation	p.Phe178CysfsTer52(p.F178Cfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373087
Start	37481629:37481630(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.614dupA
AA Mutation	p.Lys206GlufsTer20(p.K206Efs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373087
Start	37483485:37483486(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1676dupA
AA Mutation	p.Leu560AlafsTer40(p.L560Afs*40)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	24
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000373087
Start	37480311:37480313(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.467_469delCCT
AA Mutation	p.Ser156del(p.S156del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

ID	25
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000373087
Start	37483221:37483223(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1411_1413delTAC
AA Mutation	p.Tyr471del(p.Y471del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript