Colon Cancer: Gene >> IL22RA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296980
Start	137158466:137158466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78T>A
AA Mutation	p.His26Gln(p.H26Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296980
Start	137147846:137147846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518C>A
AA Mutation	p.Ser173Tyr(p.S173Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296980
Start	137154996:137154996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140915731
CDS Mutation	c.417G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296980
Start	137147789:137147789(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.575delA
AA Mutation	p.Asn192MetfsTer4(p.N192Mfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296980
Start	137147788:137147789(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs756450081
CDS Mutation	c.575dupA
AA Mutation	p.Asn192LysfsTer9(p.N192Kfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IL22RA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296980
Start	137147797:137147797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567G>T
AA Mutation	p.Lys189Asn(p.K189N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript