Colon Cancer: Gene >> C5AR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355085
Start	47320318:47320318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.541T>C
AA Mutation	p.Tyr181His(p.Y181H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355085
Start	47320099:47320099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322G>A
AA Mutation	p.Ala108Thr(p.A108T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355085
Start	47320040:47320040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201037165
CDS Mutation	c.263C>T
AA Mutation	p.Ala88Val(p.A88V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355085
Start	47320137:47320137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360G>A
AA Mutation	p.Met120Ile(p.M120I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355085
Start	47320677:47320677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140534066
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355085
Start	47320434:47320434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117536261
CDS Mutation	c.657G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> C5AR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355085
Start	47320360:47320360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770659810
CDS Mutation	c.583G>A
AA Mutation	p.Asp195Asn(p.D195N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355085
Start	47320060:47320060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283T>C
AA Mutation	p.Ser95Pro(p.S95P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript