Mutation

Primary Site >> Stomach Cancer

Gene >> CUL3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224503002:224503002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774263455
CDS Mutation	c.1448C>T
AA Mutation	p.Thr483Met(p.T483M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224511450:224511450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.787G>A
AA Mutation	p.Val263Met(p.V263M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224495918:224495918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1756A>G
AA Mutation	p.Asn586Asp(p.N586D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224535629:224535629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775935313
CDS Mutation	c.277G>A
AA Mutation	p.Val93Ile(p.V93I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224478250:224478250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2125C>T
AA Mutation	p.Arg709Trp(p.R709W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224513634:224513634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544G>A
AA Mutation	p.Ala182Thr(p.A182T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224514694:224514694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368330682
CDS Mutation	c.457C>T
AA Mutation	p.Arg153Cys(p.R153C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264414
Start	224503671:224503671(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1358delA
AA Mutation	p.Asn453ThrfsTer2(p.N453Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264414
Start	224503670:224503671(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1358dupA
AA Mutation	p.Asn453LysfsTer5(p.N453Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript