Colon Cancer: Gene >> ZFX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304543
Start	24207331:24207331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652G>A
AA Mutation	p.Asp218Asn(p.D218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304543
Start	24208926:24208926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120C>T
AA Mutation	p.Arg374Trp(p.R374W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304543
Start	24211287:24211287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2329C>T
AA Mutation	p.Arg777Trp(p.R777W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304543
Start	24210768:24210768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1810C>T
AA Mutation	p.Pro604Ser(p.P604S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304543
Start	24210833:24210833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766815041
CDS Mutation	c.1875T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304543
Start	24210701:24210701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143557208
CDS Mutation	c.1743C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304543
Start	24211223:24211223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2265C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304543
Start	24210887:24210887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369124495
CDS Mutation	c.1929G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304543
Start	24211271:24211271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150173584
CDS Mutation	c.2313G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304543
Start	24210485:24210485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304543
Start	24210493:24210493(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1539delA
AA Mutation	p.Gly514GlufsTer21(p.G514Efs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000304543
Start	24211035:24211035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2077A>T
AA Mutation	p.Arg693Ter(p.R693*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000304543
Start	24179689:24179690(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.565_566insTAATGT
AA Mutation	p.Ala189delinsValMetSer(p.A189delinsVMS)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZFX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304543
Start	24208238:24208238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961G>A
AA Mutation	p.Glu321Lys(p.E321K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304543
Start	24210887:24210887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369124495
CDS Mutation	c.1929G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000304543
Start	24207477:24207477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.796+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript