Colon Cancer: Gene >> ACAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367048
Start	159778722:159778722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087C>A
AA Mutation	p.Leu363Ile(p.L363I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367048
Start	159778816:159778816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1181T>C
AA Mutation	p.Val394Ala(p.V394A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367048
Start	159777382:159777382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748574249
CDS Mutation	c.838A>G
AA Mutation	p.Ile280Val(p.I280V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367048
Start	159778242:159778242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985G>T
AA Mutation	p.Ala329Ser(p.A329S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367048
Start	159777418:159777418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774247391
CDS Mutation	c.874A>G
AA Mutation	p.Ile292Val(p.I292V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367048
Start	159777435:159777435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367048
Start	159777434:159777435(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.890_891insG
AA Mutation	p.Ile298AsnfsTer19(p.I298Nfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367048
Start	159762988:159762989(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.126_127dupGA
AA Mutation	p.Lys43ArgfsTer49(p.K43Rfs*49)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ACAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367048
Start	159776170:159776170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655G>C
AA Mutation	p.Asp219His(p.D219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript