Colon Cancer: Gene >> TLX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370196
Start	101131623:101131623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82C>T
AA Mutation	p.Pro28Ser(p.P28S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370196
Start	101136897:101136897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.977C>T
AA Mutation	p.Ala326Val(p.A326V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370196
Start	101136891:101136891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143449957
CDS Mutation	c.971C>T
AA Mutation	p.Ser324Leu(p.S324L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370196
Start	101134220:101134220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614G>A
AA Mutation	p.Arg205His(p.R205H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370196
Start	101134234:101134234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Cys(p.R210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370196
Start	101131581:101131581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.40G>A
AA Mutation	p.Ala14Thr(p.A14T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370196
Start	101131728:101131728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187G>A
AA Mutation	p.Ala63Thr(p.A63T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370196
Start	101136733:101136733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.813G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370196
Start	101134335:101134335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.729G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370196
Start	101134329:101134329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TLX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370196
Start	101136843:101136843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923A>C
AA Mutation	p.Asn308Thr(p.N308T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370196
Start	101134196:101134196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590C>T
AA Mutation	p.Thr197Met(p.T197M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370196
Start	101134303:101134303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697G>A
AA Mutation	p.Ala233Thr(p.A233T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370196
Start	101136797:101136797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877G>A
AA Mutation	p.Ala293Thr(p.A293T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370196
Start	101134218:101134218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612G>A
Mutation Classification	Silent
Feature Type	Transcript