Colon Cancer: Gene >> CRBN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231948
Start	3174104:3174104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151127854
CDS Mutation	c.332G>A
AA Mutation	p.Arg111Gln(p.R111Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231948
Start	3172872:3172872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431A>G
AA Mutation	p.Tyr144Cys(p.Y144C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231948
Start	3156262:3156262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.707A>C
AA Mutation	p.Asn236Thr(p.N236T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231948
Start	3174243:3174243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.193G>A
AA Mutation	p.Glu65Lys(p.E65K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000231948
Start	3150920:3150920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566932471
CDS Mutation	c.1274C>T
AA Mutation	p.Thr425Met(p.T425M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000231948
Start	3151041:3151041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1153G>A
AA Mutation	p.Ala385Thr(p.A385T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000231948
Start	3174098:3174098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.338T>G
AA Mutation	p.Leu113Ter(p.L113*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000231948
Start	3154021:3154022(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.889_890insTATACAG
AA Mutation	p.Gln297LeufsTer6(p.Q297Lfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000231948
Start	3154076:3154076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.836-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CRBN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231948
Start	3174087:3174087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349G>A
AA Mutation	p.Asp117Asn(p.D117N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231948
Start	3154027:3154027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.884G>T
AA Mutation	p.Arg295Ile(p.R295I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000231948
Start	3174120:3174120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316G>T
AA Mutation	p.Glu106Ter(p.E106*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript