Colon Cancer: Gene >> RAC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306897
Start	82033588:82033588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.437C>G
AA Mutation	p.Ala146Gly(p.A146G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306897
Start	82033005:82033005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284C>T
AA Mutation	p.Ala95Val(p.A95V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306897
Start	82033821:82033821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>A
AA Mutation	p.Val191Ile(p.V191I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RAC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306897
Start	82032967:82032967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246C>A
AA Mutation	p.Phe82Leu(p.F82L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript