Colon Cancer: Gene >> RAB6B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285208
Start	133864607:133864607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106G>A
AA Mutation	p.Asp36Asn(p.D36N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285208
Start	133838213:133838213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.448G>T
AA Mutation	p.Val150Phe(p.V150F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285208
Start	133839582:133839582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769627212
CDS Mutation	c.325G>A
AA Mutation	p.Asp109Asn(p.D109N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285208
Start	133838173:133838173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488T>C
AA Mutation	p.Val163Ala(p.V163A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285208
Start	133834635:133834635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285208
Start	133839583:133839583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201173392
CDS Mutation	c.324C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000285208
Start	133895453:133895453(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.14delG
AA Mutation	p.Gly5GlufsTer7(p.G5Efs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000285208
Start	133834635:133834635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147187493
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Ter(p.R168*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000285208
Start	133838222:133838222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439G>T
AA Mutation	p.Glu147Ter(p.E147*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000285208
Start	133841387:133841387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187C>T
AA Mutation	p.Arg63Ter(p.R63*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000285208
Start	133839618:133839618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RAB6B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285208
Start	133864598:133864598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115G>A
AA Mutation	p.Asp39Asn(p.D39N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285208
Start	133864608:133864608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772849485
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000285208
Start	133834635:133834635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147187493
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Ter(p.R168*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript