Colon Cancer: Gene >> IL6R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368485
Start	154434656:154434656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.596G>A
AA Mutation	p.Gly199Glu(p.G199E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368485
Start	154465309:154465309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336A>C
AA Mutation	p.Asn446His(p.N446H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368485
Start	154429202:154429202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92C>T
AA Mutation	p.Ala31Val(p.A31V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368485
Start	154436002:154436002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>A
AA Mutation	p.Asp281Asn(p.D281N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368485
Start	154465159:154465159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186G>A
AA Mutation	p.Ala396Thr(p.A396T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368485
Start	154449932:154449932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747599074
CDS Mutation	c.1018G>A
AA Mutation	p.Asp340Asn(p.D340N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368485
Start	154430577:154430577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373789486
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IL6R

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368485
Start	154429254:154429254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript