Colon Cancer: Gene >> RAB34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301043
Start	28715088:28715088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769328864
CDS Mutation	c.548C>G
AA Mutation	p.Ala183Gly(p.A183G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301043
Start	28716038:28716038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.167T>G
AA Mutation	p.Ile56Ser(p.I56S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000301043
Start	28715703:28715703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317G>T
AA Mutation	p.Trp106Leu(p.W106L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301043
Start	28715888:28715888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226A>G
AA Mutation	p.Thr76Ala(p.T76A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000301043
Start	28714898:28714898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607G>A
AA Mutation	p.Glu203Lys(p.E203K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301043
Start	28716043:28716043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.162G>T
AA Mutation	p.Lys54Asn(p.K54N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301043
Start	28715076:28715076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560C>A
AA Mutation	p.Ala187Asp(p.A187D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000301043
Start	28714817:28714817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688G>C
AA Mutation	p.Ala230Pro(p.A230P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301043
Start	28717234:28717234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000301043
Start	28715054:28715054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.582C>A
AA Mutation	p.Tyr194Ter(p.Y194*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000301043
Start	28714886:28714886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619G>T
AA Mutation	p.Glu207Ter(p.E207*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RAB34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301043
Start	28715081:28715081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555G>T
AA Mutation	p.Gln185His(p.Q185H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301043
Start	28715670:28715670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350T>C
AA Mutation	p.Ile117Thr(p.I117T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301043
Start	28714881:28714881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624C>A
AA Mutation	p.Phe208Leu(p.F208L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript