Colon Cancer: Gene >> ZBTB22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000431845
Start	33316349:33316349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773438495
CDS Mutation	c.568C>T
AA Mutation	p.Arg190Cys(p.R190C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000431845
Start	33315424:33315424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1493G>A
AA Mutation	p.Ser498Asn(p.S498N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000431845
Start	33316391:33316391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750159071
CDS Mutation	c.526G>A
AA Mutation	p.Gly176Arg(p.G176R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000431845
Start	33316137:33316137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780G>T
AA Mutation	p.Glu260Asp(p.E260D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000431845
Start	33316729:33316729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.188T>C
AA Mutation	p.Val63Ala(p.V63A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000431845
Start	33316351:33316351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372697719
CDS Mutation	c.566C>T
AA Mutation	p.Ala189Val(p.A189V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000431845
Start	33315892:33315892(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1025delG
AA Mutation	p.Gly342ValfsTer17(p.G342Vfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000431845
Start	33315690:33315690(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1227delC
AA Mutation	p.Ser410ProfsTer45(p.S410Pfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000431845
Start	33315868:33315868(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746078084
CDS Mutation	c.1049delG
AA Mutation	p.Gly350GlufsTer9(p.G350Efs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000431845
Start	33315067:33315067(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1850delC
AA Mutation	p.Pro617HisfsTer96(p.P617Hfs*96)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZBTB22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000431845
Start	33316693:33316693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224T>C
AA Mutation	p.Leu75Pro(p.L75P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript