Colon Cancer: Gene >> IL4I1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49894384:49894384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369942631
CDS Mutation	c.451G>A
AA Mutation	p.Glu151Lys(p.E151K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49894386:49894386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449A>C
AA Mutation	p.His150Pro(p.H150P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49891457:49891457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584A>G
AA Mutation	p.Lys195Arg(p.K195R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49890233:49890233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1141C>T
AA Mutation	p.Arg381Cys(p.R381C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49890079:49890079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1295G>A
AA Mutation	p.Arg432His(p.R432H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49894287:49894287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548A>G
AA Mutation	p.Tyr183Cys(p.Y183C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49890046:49890046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1328G>A
AA Mutation	p.Arg443His(p.R443H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49896018:49896018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49A>G
AA Mutation	p.Ser17Gly(p.S17G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49895984:49895984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141664132
CDS Mutation	c.83G>A
AA Mutation	p.Arg28His(p.R28H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49889899:49889899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1475C>T
AA Mutation	p.Thr492Met(p.T492M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49889998:49889998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1376C>A
AA Mutation	p.Pro459Gln(p.P459Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391826
Start	49891042:49891042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391826
Start	49889994:49889994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1380G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391826
Start	49895845:49895845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762722182
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000391826
Start	49896055:49896055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> IL4I1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391826
Start	49895894:49895894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.173A>G
AA Mutation	p.Lys58Arg(p.K58R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391826
Start	49891411:49891411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369542657
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000391826
Start	49891091:49891092(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.652dupG
AA Mutation	p.Glu218GlyfsTer153(p.E218Gfs*153)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript