Colon Cancer: Gene >> IL22RA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270800
Start	24134281:24134281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461T>A
AA Mutation	p.Leu154Gln(p.L154Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270800
Start	24121449:24121449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750435511
CDS Mutation	c.1081C>T
AA Mutation	p.Pro361Ser(p.P361S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270800
Start	24138680:24138680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270800
Start	24121018:24121018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1512C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270800
Start	24137195:24137195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772991905
CDS Mutation	c.291C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270800
Start	24123323:24123323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145677629
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	start_lost
Transcription ID	ENST00000270800
Start	24143081:24143081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> IL22RA1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270800
Start	24138593:24138593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779925405
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript