Colon Cancer: Gene >> RIPK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259808
Start	3110911:3110911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367576973
CDS Mutation	c.1685C>T
AA Mutation	p.Thr562Met(p.T562M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259808
Start	3077840:3077840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376914574
CDS Mutation	c.226G>A
AA Mutation	p.Val76Met(p.V76M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259808
Start	3113154:3113154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1831C>G
AA Mutation	p.Gln611Glu(p.Q611E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259808
Start	3113325:3113325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755615425
CDS Mutation	c.2002G>A
AA Mutation	p.Val668Ile(p.V668I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000259808
Start	3083308:3083308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683A>G
AA Mutation	p.Tyr228Cys(p.Y228C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000259808
Start	3104240:3104240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184895368
CDS Mutation	c.931G>A
AA Mutation	p.Glu311Lys(p.E311K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259808
Start	3083231:3083231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138924769
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259808
Start	3110912:3110912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746548541
CDS Mutation	c.1686G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000259808
Start	3104264:3104264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.955C>T
AA Mutation	p.Gln319Ter(p.Q319*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000259808
Start	3110805:3110805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1579G>T
AA Mutation	p.Glu527Ter(p.E527*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RIPK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259808
Start	3106046:3106046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1571C>G
AA Mutation	p.Pro524Arg(p.P524R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript