Colon Cancer: Gene >> ZBTB32

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262630
Start	35715209:35715209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150269464
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Cys(p.R195C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262630
Start	35714919:35714919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.293G>T
AA Mutation	p.Arg98Met(p.R98M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262630
Start	35715306:35715306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755206702
CDS Mutation	c.680G>A
AA Mutation	p.Arg227His(p.R227H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262630
Start	35715305:35715305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2234366
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Cys(p.R227C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262630
Start	35715288:35715288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.662G>A
AA Mutation	p.Gly221Asp(p.G221D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262630
Start	35715290:35715290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664T>G
AA Mutation	p.Ser222Ala(p.S222A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262630
Start	35715124:35715124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753319110
CDS Mutation	c.498C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262630
Start	35715946:35715946(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.967delC
AA Mutation	p.Gln323ArgfsTer94(p.Q323Rfs*94)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000262630
Start	35714963:35714963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759629497
CDS Mutation	c.337C>T
AA Mutation	p.Arg113Ter(p.R113*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZBTB32

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262630
Start	35715033:35715033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.407G>T
AA Mutation	p.Arg136Met(p.R136M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262630
Start	35715436:35715436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810C>T
Mutation Classification	Silent
Feature Type	Transcript