Colon Cancer: Gene >> IL2RB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216223
Start	37142463:37142463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253G>A
AA Mutation	p.Ala85Thr(p.A85T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216223
Start	37143600:37143600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124G>A
AA Mutation	p.Ala42Thr(p.A42T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000216223
Start	37142510:37142510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206G>A
AA Mutation	p.Arg69Gln(p.R69Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216223
Start	37128503:37128503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768345015
CDS Mutation	c.1249G>A
AA Mutation	p.Ala417Thr(p.A417T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216223
Start	37139121:37139121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216223
Start	37143571:37143571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751954007
CDS Mutation	c.153T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216223
Start	37128714:37128714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771604727
CDS Mutation	c.1038C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216223
Start	37139196:37139196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200052713
CDS Mutation	c.309C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216223
Start	37142482:37142482(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.234delC
AA Mutation	p.Val79Ter(p.V79*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216223
Start	37128286:37128286(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1466delC
AA Mutation	p.Pro489LeufsTer43(p.P489Lfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IL2RB

No Mutation Annotation!