Colon Cancer: Gene >> ACAA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333167
Start	38136987:38136987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.49T>C
AA Mutation	p.Ser17Pro(p.S17P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333167
Start	38126311:38126311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.848C>T
AA Mutation	p.Ala283Val(p.A283V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333167
Start	38131955:38131955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374C>T
AA Mutation	p.Ser125Leu(p.S125L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333167
Start	38126264:38126264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895C>G
AA Mutation	p.Pro299Ala(p.P299A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000333167
Start	38127825:38127825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587G>A
AA Mutation	p.Arg196Gln(p.R196Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000333167
Start	38125843:38125843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1036G>A
AA Mutation	p.Glu346Lys(p.E346K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333167
Start	38125659:38125659(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1105delC
AA Mutation	p.Leu369TrpfsTer7(p.L369Wfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000333167
Start	38131594:38131594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ACAA1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333167
Start	38125853:38125853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779832294
CDS Mutation	c.1026C>T
Mutation Classification	Silent
Feature Type	Transcript