Colon Cancer: Gene >> IDH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345146
Start	208251449:208251449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781398075
CDS Mutation	c.103G>A
AA Mutation	p.Val35Met(p.V35M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345146
Start	208251455:208251455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555882127
CDS Mutation	c.97C>T
AA Mutation	p.Pro33Ser(p.P33S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345146
Start	208248406:208248406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377A>G
AA Mutation	p.Lys126Arg(p.K126R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345146
Start	208239880:208239880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974C>T
AA Mutation	p.Thr325Met(p.T325M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345146
Start	208248389:208248389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>G
AA Mutation	p.Arg132Gly(p.R132G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345146
Start	208248478:208248478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305T>C
AA Mutation	p.Ile102Thr(p.I102T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345146
Start	208243581:208243581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544A>T
AA Mutation	p.Met182Leu(p.M182L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000345146
Start	208248389:208248389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913499
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Cys(p.R132C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345146
Start	208239190:208239190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1035G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IDH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345146
Start	208239225:208239225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000T>A
AA Mutation	p.Phe334Ile(p.F334I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript