Colon Cancer: Gene >> RAB4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366690
Start	229302940:229302940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368207169
CDS Mutation	c.620G>A
AA Mutation	p.Arg207His(p.R207H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366690
Start	229299042:229299042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511G>A
AA Mutation	p.Ala171Thr(p.A171T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366690
Start	229288805:229288805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.189G>T
AA Mutation	p.Lys63Asn(p.K63N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366690
Start	229299035:229299035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.504A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366690
Start	229286557:229286558(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.111dupA
AA Mutation	p.Phe38IlefsTer4(p.F38Ifs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RAB4A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366690
Start	229297620:229297620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429A>G
Mutation Classification	Silent
Feature Type	Transcript