Colon Cancer: Gene >> RRAS

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000246792
Start	49635735:49635735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199540462
CDS Mutation	c.571C>T
AA Mutation	p.Arg191Trp(p.R191W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246792
Start	49636650:49636650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.422G>A
AA Mutation	p.Gly141Glu(p.G141E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246792
Start	49636690:49636690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Trp(p.R128W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246792
Start	49635826:49635826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246792
Start	49635594:49635594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.639C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246792
Start	49635633:49635633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183538580
CDS Mutation	c.600G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246792
Start	49635598:49635598(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.635delG
AA Mutation	p.Gly212AlafsTer22(p.G212Afs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RRAS

No Mutation Annotation!