Colon Cancer: Gene >> ELOVL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302274
Start	110059704:110059704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272C>G
AA Mutation	p.Thr91Ser(p.T91S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302274
Start	110051525:110051525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611C>T
AA Mutation	p.Thr204Ile(p.T204I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302274
Start	110051358:110051358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778A>G
AA Mutation	p.Lys260Glu(p.K260E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302274
Start	110105575:110105575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375332200
CDS Mutation	c.143G>A
AA Mutation	p.Arg48Gln(p.R48Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ELOVL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302274
Start	110059627:110059627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>C
AA Mutation	p.Val117Leu(p.V117L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302274
Start	110051446:110051446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690G>T
AA Mutation	p.Gln230His(p.Q230H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302274
Start	110051698:110051698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript