Colon Cancer: Gene >> IGDCC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65375303:65375303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.203C>T
AA Mutation	p.Thr68Ile(p.T68I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65331436:65331436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372G>A
AA Mutation	p.Val458Ile(p.V458I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65375385:65375385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121G>A
AA Mutation	p.Glu41Lys(p.E41K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65333298:65333298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941C>T
AA Mutation	p.Thr314Ile(p.T314I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65329054:65329054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374473042
CDS Mutation	c.2300C>T
AA Mutation	p.Ala767Val(p.A767V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65333262:65333262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.977T>G
AA Mutation	p.Val326Gly(p.V326G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65333271:65333271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968G>T
AA Mutation	p.Arg323Leu(p.R323L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65333276:65333276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.963G>T
AA Mutation	p.Gln321His(p.Q321H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327987
Start	65329427:65329427(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2168delC
AA Mutation	p.Pro723ArgfsTer37(p.P723Rfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327987
Start	65330738:65330738(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1565delC
AA Mutation	p.Pro522LeufsTer71(p.P522Lfs*71)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000327987
Start	65335378:65335378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598C>T
AA Mutation	p.Arg200Ter(p.R200*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000327987
Start	65330742:65330742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1562-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> IGDCC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65333329:65333329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368951025
CDS Mutation	c.910G>A
AA Mutation	p.Val304Ile(p.V304I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65335896:65335896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470G>C
AA Mutation	p.Arg157Pro(p.R157P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65332007:65332007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082T>C
AA Mutation	p.Val361Ala(p.V361A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327987
Start	65375385:65375385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121G>A
AA Mutation	p.Glu41Lys(p.E41K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript