Colon Cancer: Gene >> UEVLD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396197
Start	18558275:18558275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747008280
CDS Mutation	c.668C>T
AA Mutation	p.Thr223Met(p.T223M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000396197
Start	18578807:18578807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44A>G
AA Mutation	p.Tyr15Cys(p.Y15C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396197
Start	18578738:18578738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113C>A
AA Mutation	p.Ser38Tyr(p.S38Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396197
Start	18564963:18564963(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.541delA
AA Mutation	p.Thr181GlnfsTer19(p.T181Qfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000396197
Start	18544797:18544797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> UEVLD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396197
Start	18566452:18566452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388G>A
AA Mutation	p.Glu130Lys(p.E130K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000396197
Start	18544659:18544659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1024G>T
AA Mutation	p.Glu342Ter(p.E342*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript