Mutation

Primary Site >> Stomach Cancer

Gene >> CYP2E1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252945
Start	133533775:133533775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749979006
CDS Mutation	c.845G>A
AA Mutation	p.Arg282His(p.R282H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252945
Start	133538956:133538956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759928543
CDS Mutation	c.1474C>T
AA Mutation	p.Arg492Cys(p.R492C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252945
Start	133533789:133533789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859G>A
AA Mutation	p.Asp287Asn(p.D287N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252945
Start	133537147:133537147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1052A>G
AA Mutation	p.Asp351Gly(p.D351G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252945
Start	133527478:133527478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.83G>T
AA Mutation	p.Ser28Ile(p.S28I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252945
Start	133537149:133537149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054G>T
AA Mutation	p.Ala352Ser(p.A352S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252945
Start	133537105:133537105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759707874
CDS Mutation	c.1010G>A
AA Mutation	p.Arg337Gln(p.R337Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252945
Start	133527494:133527494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252945
Start	133537124:133537124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1029T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252945
Start	133528516:133528516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.213C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252945
Start	133532751:133532751(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.713delA
AA Mutation	p.Asn238MetfsTer5(p.N238Mfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript