Colon Cancer: Gene >> RAC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249071
Start	37232829:37232829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.197G>A
AA Mutation	p.Arg66His(p.R66H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249071
Start	37231375:37231375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304C>T
AA Mutation	p.Arg102Trp(p.R102W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249071
Start	37226690:37226690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758461304
CDS Mutation	c.562G>A
AA Mutation	p.Ala188Thr(p.A188T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249071
Start	37226736:37226736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249071
Start	37226751:37226751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79799102
CDS Mutation	c.501C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249071
Start	37231316:37231316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771516943
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000249071
Start	37231392:37231392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RAC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249071
Start	37231298:37231298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381G>T
AA Mutation	p.Glu127Asp(p.E127D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript