Colon Cancer: Gene >> IL1RN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409930
Start	113132707:113132707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45507693
CDS Mutation	c.370G>A
AA Mutation	p.Ala124Thr(p.A124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409930
Start	113131147:113131147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.308T>G
AA Mutation	p.Leu103Arg(p.L103R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409930
Start	113132720:113132720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383C>T
AA Mutation	p.Ser128Leu(p.S128L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409930
Start	113131079:113131079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.240T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IL1RN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409930
Start	113132702:113132702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373101669
CDS Mutation	c.365G>A
AA Mutation	p.Arg122His(p.R122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409930
Start	113129599:113129599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.140C>G
AA Mutation	p.Thr47Ser(p.T47S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409930
Start	113132833:113132833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143208167
CDS Mutation	c.496G>A
AA Mutation	p.Val166Ile(p.V166I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript