Colon Cancer: Gene >> ARNT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303329
Start	80552701:80552701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016C>T
AA Mutation	p.Ser339Phe(p.S339F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303329
Start	80470366:80470366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343T>C
AA Mutation	p.Ser115Pro(p.S115P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303329
Start	80470243:80470243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.220C>T
AA Mutation	p.Arg74Cys(p.R74C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303329
Start	80450984:80450984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140468271
CDS Mutation	c.136C>T
AA Mutation	p.Arg46Trp(p.R46W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303329
Start	80552700:80552700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015T>C
AA Mutation	p.Ser339Pro(p.S339P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303329
Start	80475220:80475220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619A>T
AA Mutation	p.Thr207Ser(p.T207S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303329
Start	80508233:80508233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Trp(p.R234W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303329
Start	80581307:80581307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377099665
CDS Mutation	c.1821G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303329
Start	80508232:80508232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767002088
CDS Mutation	c.699G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303329
Start	80470401:80470401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752823394
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303329
Start	80580482:80580482(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1687delA
AA Mutation	p.Ile563SerfsTer5(p.I563Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ARNT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303329
Start	80563133:80563133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768601519
CDS Mutation	c.1210C>T
AA Mutation	p.Arg404Cys(p.R404C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303329
Start	80475023:80475023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.422T>C
AA Mutation	p.Leu141Pro(p.L141P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303329
Start	80470244:80470244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221G>A
AA Mutation	p.Arg74His(p.R74H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript