Colon Cancer: Gene >> RAB7A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265062
Start	128806404:128806404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.213G>C
AA Mutation	p.Gln71His(p.Q71H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265062
Start	128806478:128806478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287T>G
AA Mutation	p.Phe96Cys(p.F96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265062
Start	128795416:128795416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.49T>C
AA Mutation	p.Ser17Pro(p.S17P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265062
Start	128806525:128806525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.334C>T
AA Mutation	p.Pro112Ser(p.P112S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265062
Start	128807627:128807627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121909079
CDS Mutation	c.484G>A
AA Mutation	p.Val162Met(p.V162M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265062
Start	128797954:128797954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.65C>T
AA Mutation	p.Thr22Ile(p.T22I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265062
Start	128797994:128797994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105T>G
AA Mutation	p.Asn35Lys(p.N35K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RAB7A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265062
Start	128806443:128806443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778176566
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript