Colon Cancer: Gene >> TSKU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333090
Start	76796539:76796539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923T>C
AA Mutation	p.Val308Ala(p.V308A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333090
Start	76795858:76795858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242C>T
AA Mutation	p.Pro81Leu(p.P81L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333090
Start	76796543:76796543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745740816
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333090
Start	76796294:76796294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772104778
CDS Mutation	c.678G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333090
Start	76796354:76796354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756652103
CDS Mutation	c.738G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333090
Start	76796075:76796075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374281937
CDS Mutation	c.459G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333090
Start	76796642:76796642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543814340
CDS Mutation	c.1026C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TSKU

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333090
Start	76796291:76796291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780198454
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000333090
Start	76796082:76796082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466C>T
AA Mutation	p.Gln156Ter(p.Q156*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript