Colon Cancer: Gene >> ACO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309951
Start	32405563:32405563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376599072
CDS Mutation	c.57G>T
AA Mutation	p.Lys19Asn(p.K19N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309951
Start	32436390:32436390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2240G>A
AA Mutation	p.Gly747Glu(p.G747E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309951
Start	32424624:32424624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147T>C
AA Mutation	p.Ser383Pro(p.S383P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309951
Start	32434661:32434661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2059G>A
AA Mutation	p.Ala687Thr(p.A687T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309951
Start	32449014:32449014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2489C>T
AA Mutation	p.Thr830Ile(p.T830I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309951
Start	32423349:32423349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001A>C
AA Mutation	p.Lys334Thr(p.K334T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309951
Start	32418192:32418192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.469T>G
AA Mutation	p.Leu157Val(p.L157V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309951
Start	32405521:32405521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772130307
CDS Mutation	c.15C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309951
Start	32418471:32418471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371235086
CDS Mutation	c.618G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309951
Start	32434574:32434574(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1976delC
AA Mutation	p.Pro659LeufsTer4(p.P659Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000309951
Start	32418180:32418180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142015075
CDS Mutation	c.457C>T
AA Mutation	p.Arg153Ter(p.R153*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309951
Start	32423347:32423348(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1005dupA
AA Mutation	p.Tyr336IlefsTer13(p.Y336Ifs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ACO1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309951
Start	32407370:32407370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751872663
CDS Mutation	c.207G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309951
Start	32431756:32431757(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1765dupA
AA Mutation	p.Ile589AsnfsTer5(p.I589Nfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript