Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IL1R1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000410023
Start	102164949:102164949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237G>T
AA Mutation	p.Glu79Asp(p.E79D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000410023
Start	102166237:102166237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611G>A
AA Mutation	p.Gly204Asp(p.G204D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000410023
Start	102176677:102176677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749524190
CDS Mutation	c.1628G>A
AA Mutation	p.Arg543Gln(p.R543Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000410023
Start	102176745:102176745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772263623
CDS Mutation	c.1696G>A
AA Mutation	p.Val566Met(p.V566M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000410023
Start	102172694:102172694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847A>G
AA Mutation	p.Asn283Asp(p.N283D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000410023
Start	102165177:102165177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359T>G
AA Mutation	p.Leu120Ter(p.L120*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL1R1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000410023
Start	102176378:102176378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1329C>G
AA Mutation	p.Asn443Lys(p.N443K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000410023
Start	102176635:102176635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1586G>T
AA Mutation	p.Arg529Met(p.R529M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000410023
Start	102176554:102176554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1505C>T
AA Mutation	p.Ser502Leu(p.S502L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript