Colon Cancer: Gene >> IDH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330062
Start	90084840:90084840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781481805
CDS Mutation	c.1247C>T
AA Mutation	p.Ala416Val(p.A416V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330062
Start	90087250:90087250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829G>A
AA Mutation	p.Asp277Asn(p.D277N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330062
Start	90088703:90088703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267606870
CDS Mutation	c.418C>T
AA Mutation	p.Arg140Trp(p.R140W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330062
Start	90084303:90084303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322T>C
AA Mutation	p.Ile441Thr(p.I441T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330062
Start	90085363:90085363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992C>T
AA Mutation	p.Thr331Met(p.T331M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330062
Start	90088477:90088477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560A>T
AA Mutation	p.Asp187Val(p.D187V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000330062
Start	90084865:90084865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1222A>G
AA Mutation	p.Ser408Gly(p.S408G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330062
Start	90088686:90088686(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747216375
CDS Mutation	c.435delG
AA Mutation	p.Thr146LeufsTer15(p.T146Lfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000330062
Start	90087129:90087129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.950C>G
AA Mutation	p.Ser317Ter(p.S317*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IDH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330062
Start	90087244:90087244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.835G>A
AA Mutation	p.Asp279Asn(p.D279N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330062
Start	90084826:90084826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1261G>A
AA Mutation	p.Gly421Ser(p.G421S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript