Colon Cancer: Gene >> ARNT

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000358595
Start	150816260:150816260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1949A>G
AA Mutation	p.Gln650Arg(p.Q650R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358595
Start	150846272:150846272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218G>T
AA Mutation	p.Arg73Leu(p.R73L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358595
Start	150817136:150817136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645T>A
AA Mutation	p.Phe549Ile(p.F549I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358595
Start	150829098:150829098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162C>T
AA Mutation	p.Pro388Ser(p.P388S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358595
Start	150842444:150842444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374278306
CDS Mutation	c.252G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358595
Start	150814126:150814126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777963072
CDS Mutation	c.2064G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358595
Start	150839543:150839543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358595
Start	150812033:150812033(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2358delC
AA Mutation	p.Ser788GlnfsTer21(p.S788Qfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000358595
Start	150842438:150842439(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.257_258insGGAAAAATACAA
AA Mutation	p.Glu87_Arg88insLysTyrLysGlu(p.E87_R88insKYKE)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARNT

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358595
Start	150817415:150817415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1524A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000358595
Start	150839596:150839596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.331G>T
AA Mutation	p.Glu111Ter(p.E111*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript