Colon Cancer: Gene >> TAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294339
Start	47220161:47220161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.555A>T
AA Mutation	p.Lys185Asn(p.K185N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294339
Start	47219901:47219901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.815G>A
AA Mutation	p.Gly272Glu(p.G272E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294339
Start	47219789:47219789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294339
Start	47220154:47220154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772071010
CDS Mutation	c.562C>T
AA Mutation	p.Arg188Trp(p.R188W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294339
Start	47219959:47219959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774469518
CDS Mutation	c.757C>T
AA Mutation	p.Arg253Trp(p.R253W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294339
Start	47219741:47219741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.975C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294339
Start	47219942:47219942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774G>A
Mutation Classification	Silent
Feature Type	Transcript