Colon Cancer: Gene >> RIPK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220751
Start	89762873:89762873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218C>A
AA Mutation	p.Ala73Asp(p.A73D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220751
Start	89789415:89789415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1218C>A
AA Mutation	p.Phe406Leu(p.F406L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220751
Start	89772796:89772796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.821C>T
AA Mutation	p.Ala274Val(p.A274V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220751
Start	89769858:89769858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570T>G
AA Mutation	p.Ile190Met(p.I190M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220751
Start	89790281:89790281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1488C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000220751
Start	89769823:89769823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Ter(p.R179*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RIPK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220751
Start	89790393:89790393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775421386
CDS Mutation	c.1600T>G
AA Mutation	p.Leu534Val(p.L534V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript