Colon Cancer: Gene >> RACGAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312377
Start	50006450:50006450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.272C>A
AA Mutation	p.Ala91Asp(p.A91D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312377
Start	50016690:50016690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202081087
CDS Mutation	c.26G>A
AA Mutation	p.Arg9Gln(p.R9Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312377
Start	50006528:50006528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.194G>A
AA Mutation	p.Arg65Gln(p.R65Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312377
Start	50005372:50005372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.309T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312377
Start	49992648:49992648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1347A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000312377
Start	49994191:49994191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752168418
CDS Mutation	c.1279C>T
AA Mutation	p.Arg427Ter(p.R427*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RACGAP1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312377
Start	49994255:49994255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1215T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312377
Start	49994462:49994463(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1091_1092delCC
AA Mutation	p.Ser364TyrfsTer8(p.S364Yfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript