Colon Cancer: Gene >> RAB4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357052
Start	40786734:40786734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500G>A
AA Mutation	p.Arg167His(p.R167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357052
Start	40786714:40786714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480G>T
AA Mutation	p.Glu160Asp(p.E160D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357052
Start	40780498:40780498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746085545
CDS Mutation	c.211C>T
AA Mutation	p.Arg71Trp(p.R71W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357052
Start	40780084:40780084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82T>C
AA Mutation	p.Phe28Leu(p.F28L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357052
Start	40783831:40783831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266A>G
AA Mutation	p.Asp89Gly(p.D89G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357052
Start	40786936:40786936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574371740
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RAB4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357052
Start	40780436:40780436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.149T>C
AA Mutation	p.Val50Ala(p.V50A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357052
Start	40780479:40780479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.192G>T
Mutation Classification	Silent
Feature Type	Transcript