Colon Cancer: Gene >> IKZF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346872
Start	39777714:39777714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186585336
CDS Mutation	c.763G>A
AA Mutation	p.Val255Ile(p.V255I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346872
Start	39832136:39832136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.23C>T
AA Mutation	p.Ala8Val(p.A8V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346872
Start	39829473:39829473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.77T>G
AA Mutation	p.Leu26Trp(p.L26W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346872
Start	39788300:39788300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667C>T
AA Mutation	p.Arg223Cys(p.R223C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000346872
Start	39766310:39766310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010T>G
AA Mutation	p.Val337Gly(p.V337G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346872
Start	39766368:39766368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952G>A
AA Mutation	p.Glu318Lys(p.E318K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346872
Start	39777761:39777761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531363291
CDS Mutation	c.716C>T
AA Mutation	p.Ala239Val(p.A239V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346872
Start	39829415:39829415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346872
Start	39766045:39766045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765182589
CDS Mutation	c.1275C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346872
Start	39765847:39765847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1473T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346872
Start	39792773:39792773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759388106
CDS Mutation	c.324C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000346872
Start	39792823:39792823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274G>T
AA Mutation	p.Glu92Ter(p.E92*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IKZF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346872
Start	39829468:39829468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82G>T
AA Mutation	p.Asp28Tyr(p.D28Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346872
Start	39791577:39791577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768846820
CDS Mutation	c.431G>A
AA Mutation	p.Arg144His(p.R144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346872
Start	39765960:39765960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1360T>G
AA Mutation	p.Cys454Gly(p.C454G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346872
Start	39791508:39791508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500T>C
AA Mutation	p.Leu167Pro(p.L167P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346872
Start	39765940:39765940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1380C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346872
Start	39777709:39777709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.768G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346872
Start	39766045:39766045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765182589
CDS Mutation	c.1275C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346872
Start	39792722:39792722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375A>G
Mutation Classification	Silent
Feature Type	Transcript