Colon Cancer: Gene >> IMPDH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326739
Start	49028493:49028493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187A>G
AA Mutation	p.Thr63Ala(p.T63A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326739
Start	49025215:49025215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1061C>T
AA Mutation	p.Ala354Val(p.A354V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000326739
Start	49026521:49026521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.908A>T
AA Mutation	p.Asn303Ile(p.N303I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326739
Start	49026972:49026972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769004042
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Cys(p.R203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326739
Start	49028492:49028492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188C>T
AA Mutation	p.Thr63Ile(p.T63I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326739
Start	49026836:49026836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377463111
CDS Mutation	c.670C>T
AA Mutation	p.Arg224Trp(p.R224W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326739
Start	49024955:49024955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326739
Start	49028487:49028487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326739
Start	49027821:49027821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530770243
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IMPDH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326739
Start	49024944:49024944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1247C>A
AA Mutation	p.Ser416Tyr(p.S416Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326739
Start	49027036:49027036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543G>T
AA Mutation	p.Lys181Asn(p.K181N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326739
Start	49028475:49028475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205C>T
AA Mutation	p.Pro69Ser(p.P69S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326739
Start	49028489:49028489(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.191delC
AA Mutation	p.Pro64HisfsTer17(p.P64Hfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript