Colon Cancer: Gene >> NPTX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306773
Start	80473436:80473436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661G>T
AA Mutation	p.Asp221Tyr(p.D221Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306773
Start	80470961:80470961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375690569
CDS Mutation	c.1151G>A
AA Mutation	p.Arg384His(p.R384H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306773
Start	80470861:80470861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768903811
CDS Mutation	c.1251C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306773
Start	80471840:80471840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151190246
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306773
Start	80475590:80475590(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.573delC
AA Mutation	p.Arg192GlyfsTer14(p.R192Gfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NPTX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306773
Start	80471022:80471022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090G>T
AA Mutation	p.Gly364Cys(p.G364C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000306773
Start	80476240:80476242(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.205_207delAAG
AA Mutation	p.Lys69del(p.K69del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript