Colon Cancer: Gene >> RAB3C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58617689:58617689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71A>T
AA Mutation	p.Asp24Val(p.D24V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58617812:58617812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.194T>A
AA Mutation	p.Ile65Asn(p.I65N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58617864:58617864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246G>T
AA Mutation	p.Gln82His(p.Q82H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58726051:58726051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775390478
CDS Mutation	c.302G>A
AA Mutation	p.Arg101His(p.R101H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58617700:58617700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82G>A
AA Mutation	p.Asp28Asn(p.D28N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58851218:58851218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551T>C
AA Mutation	p.Phe184Ser(p.F184S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58617814:58617814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196G>A
AA Mutation	p.Asp66Asn(p.D66N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58617764:58617764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146G>A
AA Mutation	p.Arg49His(p.R49H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000282878
Start	58825135:58825135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469C>T
AA Mutation	p.Arg157Ter(p.R157*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RAB3C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58851296:58851296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629A>G
AA Mutation	p.Gln210Arg(p.Q210R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58617814:58617814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196G>A
AA Mutation	p.Asp66Asn(p.D66N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58851223:58851223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199852469
CDS Mutation	c.556C>T
AA Mutation	p.Arg186Cys(p.R186C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58851244:58851244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199850819
CDS Mutation	c.577G>A
AA Mutation	p.Asp193Asn(p.D193N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282878
Start	58851304:58851304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637A>G
AA Mutation	p.Arg213Gly(p.R213G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript