Colon Cancer: Gene >> IL1RAPL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29399234:29399234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629A>G
AA Mutation	p.Asp210Gly(p.D210G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29941695:29941695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1102C>A
AA Mutation	p.Leu368Ile(p.L368I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29955570:29955570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1841C>T
AA Mutation	p.Thr614Met(p.T614M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29396388:29396388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Cys(p.R165C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29955566:29955566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1837A>T
AA Mutation	p.Asn613Tyr(p.N613Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29283081:29283081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.226T>C
AA Mutation	p.Trp76Arg(p.W76R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29955591:29955591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371810135
CDS Mutation	c.1862A>G
AA Mutation	p.Gln621Arg(p.Q621R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29283172:29283172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751673587
CDS Mutation	c.317G>A
AA Mutation	p.Arg106Gln(p.R106Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29919988:29919988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.951C>G
AA Mutation	p.Ile317Met(p.I317M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29941658:29941658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1065G>A
AA Mutation	p.Met355Ile(p.M355I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29283117:29283117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262C>A
AA Mutation	p.Pro88Thr(p.P88T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29955306:29955306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1577C>G
AA Mutation	p.Ala526Gly(p.A526G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29955389:29955389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1660C>T
AA Mutation	p.Arg554Cys(p.R554C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29955560:29955560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1831T>A
AA Mutation	p.Phe611Ile(p.F611I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29283055:29283055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200C>T
AA Mutation	p.Ala67Val(p.A67V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29396388:29396388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493C>A
AA Mutation	p.Arg165Ser(p.R165S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378993
Start	29955418:29955418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1689G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378993
Start	29668497:29668497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378993
Start	29283203:29283203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771224987
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000378993
Start	29283003:29283003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148C>T
AA Mutation	p.Arg50Ter(p.R50*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL1RAPL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29283063:29283063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208G>T
AA Mutation	p.Ala70Ser(p.A70S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378993
Start	29917544:29917544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859G>A
AA Mutation	p.Glu287Lys(p.E287K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378993
Start	29955619:29955619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764610412
CDS Mutation	c.1890C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000378993
Start	29283003:29283003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148C>T
AA Mutation	p.Arg50Ter(p.R50*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript