Colon Cancer: Gene >> ZBTB7B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292176
Start	155014832:155014832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172T>C
AA Mutation	p.Tyr58His(p.Y58H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292176
Start	155015678:155015678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018C>T
AA Mutation	p.Arg340Cys(p.R340C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292176
Start	155015526:155015526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866G>T
AA Mutation	p.Gly289Val(p.G289V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292176
Start	155015483:155015483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.823G>A
AA Mutation	p.Gly275Ser(p.G275S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292176
Start	155015138:155015138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.478C>T
AA Mutation	p.Arg160Cys(p.R160C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292176
Start	155015209:155015209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.549G>T
AA Mutation	p.Gln183His(p.Q183H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292176
Start	155016466:155016466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1401A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292176
Start	155015797:155015797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368877809
CDS Mutation	c.1137C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292176
Start	155014883:155014883(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.227delG
AA Mutation	p.Gly76ValfsTer19(p.G76Vfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292176
Start	155015396:155015396(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.740delG
AA Mutation	p.Gly247AlafsTer68(p.G247Afs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000292176
Start	155014927:155014927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267T>A
AA Mutation	p.Cys89Ter(p.C89*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion;splice_region_variant
Transcription ID	ENST00000292176
Start	155016222:155016224(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1159_1161delGAC
AA Mutation	p.Asp387del(p.D387del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZBTB7B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292176
Start	155016470:155016470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1405C>A
AA Mutation	p.Pro469Thr(p.P469T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript