Colon Cancer: Gene >> CUL7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43051703:43051703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.641A>G
AA Mutation	p.Asp214Gly(p.D214G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43052425:43052425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364C>A
AA Mutation	p.Leu122Ile(p.L122I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43045595:43045595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2854T>C
AA Mutation	p.Cys952Arg(p.C952R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43037866:43037866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773657593
CDS Mutation	c.4919G>A
AA Mutation	p.Arg1640Gln(p.R1640Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43052713:43052713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.76A>G
AA Mutation	p.Ile26Val(p.I26V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43051098:43051098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751097733
CDS Mutation	c.1103C>T
AA Mutation	p.Thr368Ile(p.T368I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43052212:43052212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369167170
CDS Mutation	c.577G>A
AA Mutation	p.Ala193Thr(p.A193T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43048389:43048389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2006T>C
AA Mutation	p.Leu669Pro(p.L669P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43037887:43037887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139249497
CDS Mutation	c.4898C>T
AA Mutation	p.Thr1633Met(p.T1633M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43042939:43042939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3508C>T
AA Mutation	p.Pro1170Ser(p.P1170S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43045308:43045308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201345667
CDS Mutation	c.2957G>A
AA Mutation	p.Arg986His(p.R986H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43038350:43038350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761970375
CDS Mutation	c.4690C>T
AA Mutation	p.Arg1564Trp(p.R1564W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43045299:43045299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2966A>G
AA Mutation	p.Tyr989Cys(p.Y989C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43038642:43038642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4491G>A
AA Mutation	p.Met1497Ile(p.M1497I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265348
Start	43050321:43050321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1311T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265348
Start	43042952:43042952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3495T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265348
Start	43048255:43048255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2064-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CUL7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43045291:43045291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2974C>T
AA Mutation	p.Arg992Trp(p.R992W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265348
Start	43045630:43045630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201130952
CDS Mutation	c.2819G>A
AA Mutation	p.Arg940His(p.R940H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000265348
Start	43049620:43049620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1612G>T
AA Mutation	p.Glu538Ter(p.E538*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265348
Start	43038693:43038693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4441-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript