Colon Cancer: Gene >> CUL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148790377:148790377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1742G>T
AA Mutation	p.Trp581Leu(p.W581L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148798006:148798006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2017C>A
AA Mutation	p.Leu673Ile(p.L673I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148730127:148730127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746247997
CDS Mutation	c.5C>T
AA Mutation	p.Ser2Leu(p.S2L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148730136:148730136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748809924
CDS Mutation	c.14G>A
AA Mutation	p.Arg5Gln(p.R5Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148783813:148783813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1114G>C
AA Mutation	p.Asp372His(p.D372H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148757104:148757104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437G>A
AA Mutation	p.Arg146His(p.R146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148799335:148799335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762885752
CDS Mutation	c.2197G>A
AA Mutation	p.Glu733Lys(p.E733K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148787038:148787038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1397A>C
AA Mutation	p.Tyr466Ser(p.Y466S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148792760:148792760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1841A>G
AA Mutation	p.Tyr614Cys(p.Y614C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148760440:148760440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733A>G
AA Mutation	p.Thr245Ala(p.T245A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325222
Start	148797823:148797823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145563536
CDS Mutation	c.1911G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325222
Start	148786586:148786589(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1336_1339delCTCA
AA Mutation	p.Leu446IlefsTer3(p.L446Ifs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000325222
Start	148790417:148790417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1782C>A
AA Mutation	p.Cys594Ter(p.C594*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000325222
Start	148800541:148800541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2290C>T
AA Mutation	p.Arg764Ter(p.R764*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000325222
Start	148799323:148799323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2185C>T
AA Mutation	p.Gln729Ter(p.Q729*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000325222
Start	148760464:148760464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757C>T
AA Mutation	p.Gln253Ter(p.Q253*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325222
Start	148783821:148783822(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1128dupA
AA Mutation	p.Tyr377IlefsTer12(p.Y377Ifs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000325222
Start	148792725:148792725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1807-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CUL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148757118:148757118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451G>A
AA Mutation	p.Glu151Lys(p.E151K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148757104:148757104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437G>A
AA Mutation	p.Arg146His(p.R146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000325222
Start	148757031:148757031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364C>T
AA Mutation	p.Gln122Ter(p.Q122*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript