Colon Cancer: Gene >> TSC22D2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361875
Start	150409587:150409587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237G>T
AA Mutation	p.Glu79Asp(p.E79D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361875
Start	150458389:150458389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2096G>T
AA Mutation	p.Ser699Ile(p.S699I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361875
Start	150410381:150410381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1031C>A
AA Mutation	p.Pro344His(p.P344H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361875
Start	150409643:150409643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293C>T
AA Mutation	p.Ala98Val(p.A98V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361875
Start	150410155:150410155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805T>G
AA Mutation	p.Phe269Val(p.F269V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361875
Start	150458497:150458497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2204C>A
AA Mutation	p.Ser735Tyr(p.S735Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361875
Start	150410184:150410184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361875
Start	150423094:150423094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2004A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361875
Start	150458583:150458583(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2290delC
AA Mutation	p.Gln764SerfsTer48(p.Q764Sfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TSC22D2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361875
Start	150458458:150458458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2165G>T
AA Mutation	p.Arg722Ile(p.R722I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript