Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IL10RB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290200
Start	33268417:33268417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs80027572
CDS Mutation	c.73G>A
AA Mutation	p.Glu25Lys(p.E25K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290200
Start	33288199:33288199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777216483
CDS Mutation	c.742G>A
AA Mutation	p.Val248Ile(p.V248I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290200
Start	33268453:33268453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109A>G
AA Mutation	p.Ile37Val(p.I37V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290200
Start	33276631:33276631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776256199
CDS Mutation	c.209C>T
AA Mutation	p.Thr70Ile(p.T70I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000290200
Start	33288184:33288184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1058861
CDS Mutation	c.727G>A
AA Mutation	p.Ala243Thr(p.A243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000290200
Start	33296287:33296287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.908A>C
AA Mutation	p.Glu303Ala(p.E303A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000290200
Start	33283187:33283187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763342351
CDS Mutation	c.592C>T
AA Mutation	p.Arg198Trp(p.R198W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290200
Start	33268512:33268512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000290200
Start	33283169:33283169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771531217
CDS Mutation	c.574C>T
AA Mutation	p.Arg192Ter(p.R192*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL10RB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290200
Start	33268417:33268417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs80027572
CDS Mutation	c.73G>A
AA Mutation	p.Glu25Lys(p.E25K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000290200
Start	33283169:33283169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771531217
CDS Mutation	c.574C>T
AA Mutation	p.Arg192Ter(p.R192*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript