Colon Cancer: Gene >> CUL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224482018:224482018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1903G>A
AA Mutation	p.Ala635Thr(p.A635T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224514709:224514709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.442C>G
AA Mutation	p.Arg148Gly(p.R148G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224514693:224514693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458G>A
AA Mutation	p.Arg153His(p.R153H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224500447:224500447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1526C>T
AA Mutation	p.Thr509Met(p.T509M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224478211:224478211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2164C>G
AA Mutation	p.Leu722Val(p.L722V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264414
Start	224481894:224481894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2027C>T
AA Mutation	p.Thr676Ile(p.T676I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224506973:224506973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750769729
CDS Mutation	c.914G>A
AA Mutation	p.Arg305His(p.R305H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224500376:224500376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772779469
CDS Mutation	c.1597G>C
AA Mutation	p.Glu533Gln(p.E533Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264414
Start	224474340:224474340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2212C>T
AA Mutation	p.Pro738Ser(p.P738S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000264414
Start	224535638:224535638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Ter(p.R90*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000264414
Start	224478307:224478307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2068G>T
AA Mutation	p.Glu690Ter(p.E690*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000264414
Start	224478347:224478347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2030-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CUL3

No Mutation Annotation!