Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258743
Start	22727608:22727608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184G>A
AA Mutation	p.Asp62Asn(p.D62N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258743
Start	22729584:22729584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.395G>T
AA Mutation	p.Arg132Ile(p.R132I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258743
Start	22731563:22731563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629G>A
AA Mutation	p.Arg210Gln(p.R210Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258743
Start	22729554:22729554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365T>G
AA Mutation	p.Phe122Cys(p.F122C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258743
Start	22728712:22728712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775325818
CDS Mutation	c.230T>C
AA Mutation	p.Met77Thr(p.M77T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258743
Start	22727596:22727596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172C>T
AA Mutation	p.Arg58Trp(p.R58W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258743
Start	22727607:22727607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140764737
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258743
Start	22727553:22727553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258743
Start	22727608:22727608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184G>A
AA Mutation	p.Asp62Asn(p.D62N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258743
Start	22727597:22727597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.173G>A
AA Mutation	p.Arg58Gln(p.R58Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258743
Start	22728753:22728753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.271A>C
AA Mutation	p.Asn91His(p.N91H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript