Colon Cancer: Gene >> CUL4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404115
Start	120544512:120544512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1106G>A
AA Mutation	p.Arg369Gln(p.R369Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404115
Start	120560137:120560137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556T>A
AA Mutation	p.Phe186Ile(p.F186I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000404115
Start	120526810:120526810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2693A>G
AA Mutation	p.Tyr898Cys(p.Y898C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000404115
Start	120536980:120536980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2047A>T
AA Mutation	p.Thr683Ser(p.T683S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000404115
Start	120560305:120560305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.388T>C
AA Mutation	p.Phe130Leu(p.F130L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000404115
Start	120540485:120540485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1575G>T
AA Mutation	p.Lys525Asn(p.K525N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000404115
Start	120534536:120534536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2265G>T
AA Mutation	p.Met755Ile(p.M755I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000404115
Start	120544506:120544506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112T>A
AA Mutation	p.Leu371His(p.L371H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404115
Start	120535857:120535857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2187C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000404115
Start	120532427:120532427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2488G>T
AA Mutation	p.Glu830Ter(p.E830*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CUL4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404115
Start	120547220:120547220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746C>A
AA Mutation	p.Ser249Tyr(p.S249Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404115
Start	120574555:120574555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769112172
CDS Mutation	c.63C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000404115
Start	120544513:120544513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105C>T
AA Mutation	p.Arg369Ter(p.R369*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000404115
Start	120539334:120539334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1729G>T
AA Mutation	p.Glu577Ter(p.E577*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript