Colon Cancer: Gene >> ZRANB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135275642:135275642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1080A>T
AA Mutation	p.Glu360Asp(p.E360D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135353460:135353460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349A>G
AA Mutation	p.Thr117Ala(p.T117A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135504459:135504459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31C>T
AA Mutation	p.Leu11Phe(p.L11F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135313523:135313523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.932T>A
AA Mutation	p.Ile311Lys(p.I311K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135315394:135315394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Cys(p.R272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135207796:135207796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2647C>T
AA Mutation	p.Pro883Ser(p.P883S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135265549:135265549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1524A>C
AA Mutation	p.Glu508Asp(p.E508D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135207516:135207516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2927T>G
AA Mutation	p.Phe976Cys(p.F976C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135315496:135315496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712G>A
AA Mutation	p.Gly238Arg(p.G238R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135350027:135350027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.548C>T
AA Mutation	p.Ala183Val(p.A183V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135227877:135227877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2093C>T
AA Mutation	p.Ala698Val(p.A698V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135353461:135353461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348A>C
AA Mutation	p.Lys116Asn(p.K116N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135269120:135269120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1228A>C
AA Mutation	p.Ser410Arg(p.S410R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135271779:135271779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1195G>C
AA Mutation	p.Ala399Pro(p.A399P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264159
Start	135200384:135200384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3198A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264159
Start	135200356:135200356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3226T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264159
Start	135230870:135230870(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs765112091
CDS Mutation	c.1597delA
AA Mutation	p.Arg533AspfsTer3(p.R533Dfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000264159
Start	135207604:135207604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367951058
CDS Mutation	c.2839C>T
AA Mutation	p.Arg947Ter(p.R947*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000264159
Start	135315531:135315531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ZRANB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135207802:135207802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2641C>A
AA Mutation	p.Leu881Ile(p.L881I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264159
Start	135230924:135230924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373989017
CDS Mutation	c.1543G>A
AA Mutation	p.Glu515Lys(p.E515K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264159
Start	135227948:135227948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2022C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000264159
Start	135207604:135207604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367951058
CDS Mutation	c.2839C>T
AA Mutation	p.Arg947Ter(p.R947*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript