Mutation

Primary Site >> Stomach Cancer

Gene >> CUL5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393094
Start	108049986:108049986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331T>C
AA Mutation	p.Phe111Leu(p.F111L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393094
Start	108089583:108089583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1403C>T
AA Mutation	p.Ala468Val(p.A468V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393094
Start	108097664:108097664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1934G>A
AA Mutation	p.Arg645Gln(p.R645Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393094
Start	108054933:108054933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183961591
CDS Mutation	c.758G>A
AA Mutation	p.Arg253Gln(p.R253Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393094
Start	108046323:108046323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188A>G
AA Mutation	p.Gln63Arg(p.Q63R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393094
Start	108094418:108094418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1471A>G
AA Mutation	p.Asn491Asp(p.N491D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000393094
Start	108104325:108104325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2284G>A
AA Mutation	p.Glu762Lys(p.E762K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000393094
Start	108054904:108054904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.729A>T
AA Mutation	p.Lys243Asn(p.K243N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000393094
Start	108094821:108094821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1577T>C
AA Mutation	p.Val526Ala(p.V526A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000393094
Start	108049955:108049955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300C>A
AA Mutation	p.Phe100Leu(p.F100L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393094
Start	108088591:108088591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393094
Start	108054946:108054946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147410964
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393094
Start	108094931:108094931(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1694delA
AA Mutation	p.Asn565IlefsTer18(p.N565Ifs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393094
Start	108089526:108089526(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1350delT
AA Mutation	p.Phe450LeufsTer2(p.F450Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000393094
Start	108098485:108098485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2104G>T
AA Mutation	p.Glu702Ter(p.E702*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000393094
Start	108073478:108073480(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1096_1098delCTT
AA Mutation	p.Leu366del(p.L366del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript