Colon Cancer: Gene >> ELOVL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372458
Start	43363968:43363968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788G>A
AA Mutation	p.Arg263His(p.R263H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372458
Start	43364341:43364341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601A>G
AA Mutation	p.Met201Val(p.M201V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372458
Start	43365280:43365280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754465886
CDS Mutation	c.143G>A
AA Mutation	p.Arg48His(p.R48H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372458
Start	43364788:43364788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201783931
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Trp(p.R109W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372458
Start	43364072:43364072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684G>C
AA Mutation	p.Gln228His(p.Q228H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_lost
Transcription ID	ENST00000372458
Start	43363918:43363918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838T>C
AA Mutation	p.Ter280ArgextTer6(p.*280Rext*6)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ELOVL1

No Mutation Annotation!