Colon Cancer: Gene >> MXD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264444
Start	69935428:69935428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767887648
CDS Mutation	c.281C>T
AA Mutation	p.Thr94Met(p.T94M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264444
Start	69938114:69938114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185788603
CDS Mutation	c.496G>A
AA Mutation	p.Val166Met(p.V166M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264444
Start	69915390:69915390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.60G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264444
Start	69916147:69916147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372453774
CDS Mutation	c.100T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000264444
Start	69921749:69921749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187G>T
AA Mutation	p.Glu63Ter(p.E63*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000264444
Start	69935418:69935418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Ter(p.R91*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MXD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264444
Start	69938105:69938105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535119144
CDS Mutation	c.487G>A
AA Mutation	p.Asp163Asn(p.D163N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000264444
Start	69935418:69935418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Ter(p.R91*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript