Colon Cancer: Gene >> IL17RA

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000319363
Start	17102139:17102139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599G>A
AA Mutation	p.Gly200Asp(p.G200D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319363
Start	17108576:17108576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772844479
CDS Mutation	c.1357G>A
AA Mutation	p.Ala453Thr(p.A453T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319363
Start	17100358:17100358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145378071
CDS Mutation	c.427C>T
AA Mutation	p.Arg143Cys(p.R143C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319363
Start	17109654:17109654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2435A>G
AA Mutation	p.Glu812Gly(p.E812G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319363
Start	17102026:17102026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151220068
CDS Mutation	c.581C>T
AA Mutation	p.Thr194Met(p.T194M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319363
Start	17103542:17103542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811C>T
AA Mutation	p.Arg271Cys(p.R271C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000319363
Start	17109081:17109081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200201810
CDS Mutation	c.1862C>T
AA Mutation	p.Ala621Val(p.A621V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319363
Start	17109469:17109469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2250C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319363
Start	17109532:17109532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2313C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319363
Start	17109514:17109514(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2300delG
AA Mutation	p.Gly767AlafsTer70(p.G767Afs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000319363
Start	17098805:17098805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.341T>A
AA Mutation	p.Leu114Ter(p.L114*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319363
Start	17109513:17109514(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2300dupG
AA Mutation	p.Cys768LeufsTer3(p.C768Lfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IL17RA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319363
Start	17104774:17104774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781461932
CDS Mutation	c.895G>A
AA Mutation	p.Ala299Thr(p.A299T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319363
Start	17109448:17109448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2229C>T
Mutation Classification	Silent
Feature Type	Transcript