Colon Cancer: Gene >> IFNAR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342136
Start	33246798:33246798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302G>A
AA Mutation	p.Ser101Asn(p.S101N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342136
Start	33263372:33263372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768028214
CDS Mutation	c.1420G>A
AA Mutation	p.Gly474Arg(p.G474R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342136
Start	33262869:33262869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.917A>C
AA Mutation	p.Tyr306Ser(p.Y306S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342136
Start	33260686:33260686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.799A>G
AA Mutation	p.Ile267Val(p.I267V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000342136
Start	33262861:33262861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.909G>T
AA Mutation	p.Glu303Asp(p.E303D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342136
Start	33262985:33262985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342136
Start	33260667:33260667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342136
Start	33260724:33260724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IFNAR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342136
Start	33263294:33263294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1342A>C
AA Mutation	p.Met448Leu(p.M448L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342136
Start	33244979:33244979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.126G>T
AA Mutation	p.Lys42Asn(p.K42N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342136
Start	33263089:33263089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1137G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342136
Start	33260655:33260655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768C>A
Mutation Classification	Silent
Feature Type	Transcript