Colon Cancer: Gene >> EVL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000402714
Start	100097551:100097551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245G>T
AA Mutation	p.Arg82Leu(p.R82L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000402714
Start	100123554:100123554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770493838
CDS Mutation	c.368G>A
AA Mutation	p.Arg123His(p.R123H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000402714
Start	100128600:100128600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367737727
CDS Mutation	c.563C>T
AA Mutation	p.Pro188Leu(p.P188L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000402714
Start	100126736:100126736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750787699
CDS Mutation	c.446G>A
AA Mutation	p.Arg149His(p.R149H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000402714
Start	100137798:100137798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1084T>C
AA Mutation	p.Ser362Pro(p.S362P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000402714
Start	100143733:100143733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1246A>G
AA Mutation	p.Thr416Ala(p.T416A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000402714
Start	100129572:100129572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368376778
CDS Mutation	c.721G>A
AA Mutation	p.Ala241Thr(p.A241T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402714
Start	100128589:100128590(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.559_560dupCC
AA Mutation	p.Pro188HisfsTer41(p.P188Hfs*41)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EVL

No Mutation Annotation!