Colon Cancer: Gene >> IL1RL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102338903:102338903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128G>A
AA Mutation	p.Ser43Asn(p.S43N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102351572:102351572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322G>C
AA Mutation	p.Ser441Thr(p.S441T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102349211:102349211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769757624
CDS Mutation	c.1250T>C
AA Mutation	p.Leu417Ser(p.L417S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102338322:102338322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58T>G
AA Mutation	p.Phe20Val(p.F20V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102340700:102340700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772536038
CDS Mutation	c.482C>T
AA Mutation	p.Ala161Val(p.A161V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102347998:102347998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024C>A
AA Mutation	p.Leu342Ile(p.L342I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102340106:102340106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281T>A
AA Mutation	p.Phe94Tyr(p.F94Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102340799:102340799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770476261
CDS Mutation	c.581T>C
AA Mutation	p.Val194Ala(p.V194A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102343301:102343301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856G>A
AA Mutation	p.Val286Ile(p.V286I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102338850:102338850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75G>T
AA Mutation	p.Trp25Cys(p.W25C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102351831:102351831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1581C>A
AA Mutation	p.Phe527Leu(p.F527L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102349127:102349127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1166C>T
AA Mutation	p.Ser389Phe(p.S389F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102343063:102343063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.710C>A
AA Mutation	p.Ala237Asp(p.A237D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233954
Start	102351831:102351831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1581C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233954
Start	102340818:102340818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233954
Start	102351708:102351708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545075452
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IL1RL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102347975:102347975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1001C>T
AA Mutation	p.Ala334Val(p.A334V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102348060:102348060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1086A>C
AA Mutation	p.Arg362Ser(p.R362S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102340165:102340165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340C>A
AA Mutation	p.Pro114Thr(p.P114T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233954
Start	102351611:102351611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1361A>G
AA Mutation	p.His454Arg(p.H454R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233954
Start	102349200:102349200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1239T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233954
Start	102343282:102343282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript