Colon Cancer: Gene >> IL2RA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379959
Start	6019915:6019915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370516220
CDS Mutation	c.610G>A
AA Mutation	p.Glu204Lys(p.E204K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379959
Start	6025934:6025934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156G>T
AA Mutation	p.Lys52Asn(p.K52N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379959
Start	6025869:6025869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756444069
CDS Mutation	c.221C>T
AA Mutation	p.Ser74Leu(p.S74L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379959
Start	6021635:6021635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763915787
CDS Mutation	c.426C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379959
Start	6025910:6025910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs74162093
CDS Mutation	c.180C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000379959
Start	6024289:6024289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322G>T
AA Mutation	p.Glu108Ter(p.E108*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL2RA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379959
Start	6021604:6021604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201188114
CDS Mutation	c.457G>A
AA Mutation	p.Val153Ile(p.V153I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379959
Start	6021635:6021635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763915787
CDS Mutation	c.426C>T
Mutation Classification	Silent
Feature Type	Transcript