Colon Cancer: Gene >> IARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375643
Start	92280802:92280802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.689T>G
AA Mutation	p.Leu230Arg(p.L230R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375643
Start	92280883:92280883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.608A>C
AA Mutation	p.Asp203Ala(p.D203A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375643
Start	92223375:92223375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3524A>G
AA Mutation	p.Asn1175Ser(p.N1175S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375643
Start	92265098:92265098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371250371
CDS Mutation	c.1531C>T
AA Mutation	p.Arg511Cys(p.R511C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375643
Start	92278238:92278238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794C>T
AA Mutation	p.Ala265Val(p.A265V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375643
Start	92268274:92268274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200389880
CDS Mutation	c.1331G>A
AA Mutation	p.Arg444Gln(p.R444Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375643
Start	92269905:92269905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1284G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375643
Start	92210870:92210870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777464643
CDS Mutation	c.3726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375643
Start	92249906:92249906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2568T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375643
Start	92260221:92260221(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1801delA
AA Mutation	p.Met601Ter(p.M601*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000375643
Start	92287827:92287827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.360C>A
AA Mutation	p.Cys120Ter(p.C120*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375643
Start	92277882:92277883(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.874dupC
AA Mutation	p.Leu292ProfsTer3(p.L292Pfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375643
Start	92268275:92268276(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1329dupA
AA Mutation	p.Arg444ThrfsTer11(p.R444Tfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375643
Start	92242320:92242320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3011T>G
AA Mutation	p.Val1004Gly(p.V1004G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375643
Start	92265034:92265034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1595G>A
AA Mutation	p.Ser532Asn(p.S532N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript