Colon Cancer: Gene >> VPS4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238497
Start	63400649:63400649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539A>C
AA Mutation	p.Lys180Thr(p.K180T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000238497
Start	63403724:63403724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467T>G
AA Mutation	p.Phe156Cys(p.F156C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000238497
Start	63411478:63411478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128A>G
AA Mutation	p.His43Arg(p.H43R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238497
Start	63393430:63393430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238497
Start	63400672:63400672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VPS4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238497
Start	63403808:63403808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373315578
CDS Mutation	c.383G>A
AA Mutation	p.Arg128Gln(p.R128Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000238497
Start	63393533:63393533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147130607
CDS Mutation	c.1109G>A
AA Mutation	p.Arg370Gln(p.R370Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript