Colon Cancer: Gene >> TDO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155914406:155914406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810G>T
AA Mutation	p.Glu270Asp(p.E270D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155904063:155904063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.81A>T
AA Mutation	p.Lys27Asn(p.K27N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155914366:155914366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770T>C
AA Mutation	p.Phe257Ser(p.F257S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155910093:155910093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500T>C
AA Mutation	p.Val167Ala(p.V167A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155905086:155905086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161C>T
AA Mutation	p.Ala54Val(p.A54V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155910106:155910106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513G>A
AA Mutation	p.Met171Ile(p.M171I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155905136:155905136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211C>A
AA Mutation	p.Leu71Ile(p.L71I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155919862:155919862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093T>G
AA Mutation	p.Leu365Val(p.L365V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155918164:155918164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.992T>G
AA Mutation	p.Met331Arg(p.M331R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000536354
Start	155914370:155914370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TDO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155904085:155904085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.103G>A
AA Mutation	p.Ala35Thr(p.A35T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155910085:155910085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492G>T
AA Mutation	p.Lys164Asn(p.K164N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155914359:155914359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.763G>C
AA Mutation	p.Ala255Pro(p.A255P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155910197:155910197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604C>A
AA Mutation	p.Leu202Met(p.L202M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155904100:155904100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.118C>A
AA Mutation	p.Leu40Ile(p.L40I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000536354
Start	155911510:155911510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632G>T
AA Mutation	p.Arg211Ile(p.R211I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript