Colon Cancer: Gene >> C1QA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374642
Start	22639057:22639057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568891417
CDS Mutation	c.388G>A
AA Mutation	p.Val130Met(p.V130M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374642
Start	22639223:22639223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554G>A
AA Mutation	p.Arg185His(p.R185H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374642
Start	22638854:22638854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.185G>T
AA Mutation	p.Gly62Val(p.G62V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374642
Start	22639122:22639122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374642
Start	22639365:22639365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761882792
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374642
Start	22639322:22639322(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.657delA
AA Mutation	p.Asp220ThrfsTer62(p.D220Tfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374642
Start	22638936:22638936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.271delC
AA Mutation	p.Leu91SerfsTer191(p.L91Sfs*191)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> C1QA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374642
Start	22639030:22639030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Trp(p.R121W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript