Colon Cancer: Gene >> RHOC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285735
Start	112702613:112702613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>A
AA Mutation	p.Asp120Asn(p.D120N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285735
Start	112703083:112703083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.193G>T
AA Mutation	p.Asp65Tyr(p.D65Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285735
Start	112701596:112701596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766734264
CDS Mutation	c.526C>T
AA Mutation	p.Arg176Trp(p.R176W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285735
Start	112703718:112703718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82G>T
AA Mutation	p.Asp28Tyr(p.D28Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285735
Start	112703707:112703707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372772606
CDS Mutation	c.93G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285735
Start	112702599:112702599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138595121
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RHOC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285735
Start	112701620:112701620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779520374
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Trp(p.R168W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript