Colon Cancer: Gene >> IKZF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50376695:50376695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323G>A
AA Mutation	p.Gly108Glu(p.G108E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50399995:50399995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928G>A
AA Mutation	p.Val310Met(p.V310M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50400520:50400520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1453G>A
AA Mutation	p.Gly485Ser(p.G485S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50400563:50400563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1496G>A
AA Mutation	p.Ser499Asn(p.S499N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50387364:50387364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.609T>G
AA Mutation	p.Cys203Trp(p.C203W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50400521:50400521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1454G>A
AA Mutation	p.Gly485Asp(p.G485D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50391740:50391740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>A
AA Mutation	p.Glu243Lys(p.E243K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50400049:50400049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.982C>T
AA Mutation	p.Arg328Cys(p.R328C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50376662:50376662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290G>T
AA Mutation	p.Arg97Met(p.R97M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50400081:50400081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775109088
CDS Mutation	c.1014C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50387424:50387424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50400474:50400474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1407G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50376576:50376576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000331340
Start	50376794:50376794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> IKZF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331340
Start	50319098:50319098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37T>A
AA Mutation	p.Ser13Thr(p.S13T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50382643:50382643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331340
Start	50376735:50376735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript