Colon Cancer: Gene >> TGFBI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442011
Start	136055708:136055708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192398905
CDS Mutation	c.1439C>T
AA Mutation	p.Ala480Val(p.A480V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442011
Start	136054856:136054856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759370852
CDS Mutation	c.1405C>T
AA Mutation	p.Arg469Cys(p.R469C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000442011
Start	136056781:136056781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121909209
CDS Mutation	c.1664G>A
AA Mutation	p.Arg555Gln(p.R555Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000442011
Start	136052969:136052969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976T>C
AA Mutation	p.Ser326Pro(p.S326P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000442011
Start	136053042:136053042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769820632
CDS Mutation	c.1049C>T
AA Mutation	p.Ala350Val(p.A350V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000442011
Start	136047317:136047317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.668A>G
AA Mutation	p.His223Arg(p.H223R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442011
Start	136052956:136052956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373071121
CDS Mutation	c.963C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442011
Start	136033769:136033769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368854767
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442011
Start	136053076:136053076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199645034
CDS Mutation	c.1083C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442011
Start	136049495:136049495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781740702
CDS Mutation	c.828G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TGFBI

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442011
Start	136047396:136047396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772472646
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript