Colon Cancer: Gene >> RHOH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381799
Start	40243916:40243916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530G>A
AA Mutation	p.Arg177Gln(p.R177Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381799
Start	40243804:40243804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.418G>T
AA Mutation	p.Ala140Ser(p.A140S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381799
Start	40243420:40243420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762307722
CDS Mutation	c.34G>A
AA Mutation	p.Asp12Asn(p.D12N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381799
Start	40243533:40243533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755150668
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381799
Start	40243632:40243632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381799
Start	40243575:40243575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.189C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381799
Start	40243407:40243407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373809098
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381799
Start	40243506:40243506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RHOH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381799
Start	40243609:40243609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.223C>A
AA Mutation	p.Gln75Lys(p.Q75K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript