Colon Cancer: Gene >> IKZF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000434687
Start	213022009:213022009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696G>T
AA Mutation	p.Gln232His(p.Q232H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000434687
Start	213148616:213148616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14C>T
AA Mutation	p.Ala5Val(p.A5V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000434687
Start	213049743:213049743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>A
AA Mutation	p.Ala182Thr(p.A182T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000434687
Start	213056991:213056991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761250260
CDS Mutation	c.248C>T
AA Mutation	p.Pro83Leu(p.P83L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000434687
Start	213056910:213056910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329G>T
AA Mutation	p.Gly110Val(p.G110V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000434687
Start	213056911:213056911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328G>T
AA Mutation	p.Gly110Cys(p.G110C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000434687
Start	213022083:213022083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622C>T
AA Mutation	p.Arg208Cys(p.R208C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000434687
Start	213007451:213007451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1490A>G
AA Mutation	p.Asp497Gly(p.D497G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000434687
Start	213008066:213008066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875T>C
AA Mutation	p.Phe292Ser(p.F292S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434687
Start	213056936:213056936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434687
Start	213007561:213007561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1380C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434687
Start	213013909:213013909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000434687
Start	213013848:213013848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799G>T
AA Mutation	p.Glu267Ter(p.E267*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000434687
Start	213007383:213007383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1558C>T
AA Mutation	p.Arg520Ter(p.R520*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000434687
Start	213007767:213007767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174C>T
AA Mutation	p.Arg392Ter(p.R392*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IKZF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000434687
Start	213013880:213013880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767C>A
AA Mutation	p.Ser256Tyr(p.S256Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript