Mutation

Primary Site >> Stomach Cancer

Gene >> ETV6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11885941:11885941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1168A>G
AA Mutation	p.Thr390Ala(p.T390A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11853484:11853484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386T>C
AA Mutation	p.Leu129Pro(p.L129P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11885945:11885945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172A>G
AA Mutation	p.Tyr391Cys(p.Y391C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11890985:11890985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1298G>A
AA Mutation	p.Arg433His(p.R433H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11869556:11869556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747770209
CDS Mutation	c.596G>A
AA Mutation	p.Arg199Gln(p.R199Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11839301:11839301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325T>G
AA Mutation	p.Ser109Ala(p.S109A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11869592:11869592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111871763
CDS Mutation	c.632G>A
AA Mutation	p.Arg211His(p.R211H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000396373
Start	11752579:11752579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750795092
CDS Mutation	c.163C>T
AA Mutation	p.Arg55Cys(p.R55C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000396373
Start	11869501:11869501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149660037
CDS Mutation	c.541C>T
AA Mutation	p.Arg181Cys(p.R181C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396373
Start	11869569:11869569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396373
Start	11869568:11869568(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.613delC
AA Mutation	p.Leu205TrpfsTer4(p.L205Wfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000396373
Start	11885901:11885942(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1153-23_1171delCCCTTCCTCCTTTGAACAAACAGAACAGAACAAACATGACCT
Mutation Classification	Splice_Site
Feature Type	Transcript