Colon Cancer: Gene >> IDH3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299518
Start	78160162:78160162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.245C>T
AA Mutation	p.Ser82Leu(p.S82L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299518
Start	78162363:78162363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607A>G
AA Mutation	p.Ile203Val(p.I203V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000299518
Start	78163508:78163508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613C>T
AA Mutation	p.Arg205Trp(p.R205W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299518
Start	78162313:78162313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557A>G
AA Mutation	p.Tyr186Cys(p.Y186C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299518
Start	78165072:78165072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.860A>G
AA Mutation	p.Glu287Gly(p.E287G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;frameshift_variant;splice_region_variant
Transcription ID	ENST00000299518
Start	78155274:78155275(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.89_90insATGGTAA
AA Mutation	p.Val31TrpfsTer2(p.V31Wfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299518
Start	78166206:78166207(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.921_922insTT
AA Mutation	p.Leu308PhefsTer6(p.L308Ffs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299518
Start	78166208:78166209(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.924_925insGG
AA Mutation	p.Leu309GlyfsTer5(p.L309Gfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IDH3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299518
Start	78161646:78161646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355G>T
AA Mutation	p.Asp119Tyr(p.D119Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299518
Start	78168994:78168994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090G>T
AA Mutation	p.Asp364Tyr(p.D364Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299518
Start	78163525:78163525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630T>G
Mutation Classification	Silent
Feature Type	Transcript