Colon Cancer: Gene >> ACP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218758
Start	11575150:11575150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838C>A
AA Mutation	p.Arg280Ser(p.R280S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218758
Start	11577151:11577151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.167G>A
AA Mutation	p.Arg56Gln(p.R56Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000218758
Start	11575029:11575029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745604493
CDS Mutation	c.959C>T
AA Mutation	p.Pro320Leu(p.P320L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000218758
Start	11575147:11575147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841T>C
AA Mutation	p.Phe281Leu(p.F281L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000218758
Start	11576400:11576400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756201795
CDS Mutation	c.578C>T
AA Mutation	p.Ala193Val(p.A193V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000218758
Start	11576452:11576452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526C>T
AA Mutation	p.Arg176Ter(p.R176*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ACP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218758
Start	11576789:11576789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148219285
CDS Mutation	c.316G>A
AA Mutation	p.Val106Met(p.V106M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript