Colon Cancer: Gene >> CUL2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374748
Start	35031619:35031619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171C>T
AA Mutation	p.Leu391Phe(p.L391F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35049707:35049707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140997018
CDS Mutation	c.482G>A
AA Mutation	p.Arg161Gln(p.R161Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35063054:35063054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128A>G
AA Mutation	p.Tyr43Cys(p.Y43C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35028821:35028821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1606A>G
AA Mutation	p.Ser536Gly(p.S536G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35028880:35028880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547C>T
AA Mutation	p.Ala516Val(p.A516V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35031361:35031361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1325G>A
AA Mutation	p.Arg442His(p.R442H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35031338:35031338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348T>C
AA Mutation	p.Ser450Pro(p.S450P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35031338:35031338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348T>G
AA Mutation	p.Ser450Ala(p.S450A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374748
Start	35054491:35054491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751929559
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374748
Start	35010314:35010314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2235G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374748
Start	35033175:35033175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768731643
CDS Mutation	c.1101G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374748
Start	35011952:35011953(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2001_2002delGA
AA Mutation	p.Gln667HisfsTer2(p.Q667Hfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000374748
Start	35039052:35039052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Ter(p.R249*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CUL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35071205:35071205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113G>A
AA Mutation	p.Arg38His(p.R38H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35038965:35038965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832T>G
AA Mutation	p.Leu278Val(p.L278V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35060940:35060940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.251T>A
AA Mutation	p.Leu84His(p.L84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35039051:35039051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.746G>A
AA Mutation	p.Arg249Gln(p.R249Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374748
Start	35011898:35011898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772665111
CDS Mutation	c.2056C>T
AA Mutation	p.Arg686Cys(p.R686C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374748
Start	35010317:35010317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770061112
CDS Mutation	c.2232C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000374748
Start	35011918:35011919(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2035_2036insG
AA Mutation	p.Tyr679Ter(p.Y679*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000374748
Start	35039052:35039052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Ter(p.R249*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript