Colon Cancer: Gene >> TLX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233638
Start	74515711:74515711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479C>T
AA Mutation	p.Pro160Leu(p.P160L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233638
Start	74515827:74515827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568571616
CDS Mutation	c.595G>A
AA Mutation	p.Ala199Thr(p.A199T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233638
Start	74515765:74515765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533G>A
AA Mutation	p.Arg178His(p.R178H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233638
Start	74514870:74514870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.64G>A
AA Mutation	p.Asp22Asn(p.D22N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233638
Start	74515785:74515785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773898981
CDS Mutation	c.553G>A
AA Mutation	p.Ala185Thr(p.A185T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000233638
Start	74516184:74516184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850G>T
AA Mutation	p.Val284Leu(p.V284L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233638
Start	74514884:74514884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000233638
Start	74515092:74515092(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.292delG
AA Mutation	p.Ala98ArgfsTer16(p.A98Rfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TLX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233638
Start	74514993:74514993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187G>A
AA Mutation	p.Ala63Thr(p.A63T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript