Colon Cancer: Gene >> DIRAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323469
Start	2717737:2717737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70G>T
AA Mutation	p.Val24Leu(p.V24L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323469
Start	2717673:2717673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>A
AA Mutation	p.Arg45Gln(p.R45Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323469
Start	2717424:2717424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>A
AA Mutation	p.Arg128Gln(p.R128Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323469
Start	2717215:2717215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592A>G
AA Mutation	p.Met198Val(p.M198V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323469
Start	2717755:2717755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52G>A
AA Mutation	p.Val18Met(p.V18M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323469
Start	2717759:2717759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323469
Start	2717495:2717495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DIRAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323469
Start	2717451:2717451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356T>A
AA Mutation	p.Val119Glu(p.V119E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript