Colon Cancer: Gene >> ZBTB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325144
Start	151366726:151366726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191541534
CDS Mutation	c.340G>A
AA Mutation	p.Ala114Thr(p.A114T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325144
Start	151366431:151366431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762417728
CDS Mutation	c.635C>T
AA Mutation	p.Pro212Leu(p.P212L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325144
Start	151366556:151366556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>T
AA Mutation	p.Gln170His(p.Q170H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325144
Start	151366504:151366504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562A>T
AA Mutation	p.Asn188Tyr(p.N188Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325144
Start	151366795:151366795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>A
AA Mutation	p.Asp91Asn(p.D91N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325144
Start	151366298:151366298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564515254
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325144
Start	151373557:151373557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771652540
CDS Mutation	c.81G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325144
Start	151365629:151365629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549133340
CDS Mutation	c.1437C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325144
Start	151365638:151365638(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1428delT
AA Mutation	p.Phe476LeufsTer3(p.F476Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZBTB2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325144
Start	151366409:151366409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.657G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325144
Start	151373548:151373548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript