Colon Cancer: Gene >> IL23R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347310
Start	67258638:67258638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772901651
CDS Mutation	c.1400C>T
AA Mutation	p.Ser467Leu(p.S467L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347310
Start	67258800:67258800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1562A>T
AA Mutation	p.Asn521Ile(p.N521I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347310
Start	67200846:67200846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758690026
CDS Mutation	c.601G>A
AA Mutation	p.Ala201Thr(p.A201T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347310
Start	67258615:67258615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347310
Start	67255841:67255841(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1156delA
AA Mutation	p.Arg386GlufsTer6(p.R386Efs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IL23R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347310
Start	67182850:67182850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382C>T
AA Mutation	p.Pro128Ser(p.P128S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000347310
Start	67219580:67219580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805G>T
AA Mutation	p.Glu269Ter(p.E269*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript