Mutation

Primary Site >> Stomach Cancer

Gene >> IKZF1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50327679:50327679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778910457
CDS Mutation	c.82G>A
AA Mutation	p.Asp28Asn(p.D28N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50327710:50327710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113C>T
AA Mutation	p.Ser38Phe(p.S38F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50400610:50400610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1543C>T
AA Mutation	p.Arg515Cys(p.R515C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50376715:50376715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343G>A
AA Mutation	p.Gly115Arg(p.G115R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50376578:50376578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144637662
CDS Mutation	c.206G>A
AA Mutation	p.Arg69His(p.R69H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50400332:50400332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375321410
CDS Mutation	c.1265C>T
AA Mutation	p.Ala422Val(p.A422V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50400410:50400410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1343C>T
AA Mutation	p.Ala448Val(p.A448V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50400340:50400340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273G>A
AA Mutation	p.Gly425Arg(p.G425R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50399976:50399976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.909C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50391826:50391826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375111826
CDS Mutation	c.813C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50400585:50400585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1518G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50382676:50382676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368759855
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50400408:50400408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143013761
CDS Mutation	c.1341C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50400588:50400588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1521G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50376609:50376609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756261862
CDS Mutation	c.237G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50391772:50391772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.759G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50382658:50382658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331340
Start	50400067:50400067(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1004delC
AA Mutation	p.Pro335ArgfsTer80(p.P335Rfs*80)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	start_lost
Transcription ID	ENST00000331340
Start	50319064:50319064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3G>T
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript