Colon Cancer: Gene >> DNAJA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330899
Start	33030446:33030446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Gly141Glu(p.G141E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330899
Start	33030557:33030557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.533T>C
AA Mutation	p.Met178Thr(p.M178T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330899
Start	33030470:33030470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446G>A
AA Mutation	p.Cys149Tyr(p.C149Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330899
Start	33038829:33038829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141132012
CDS Mutation	c.1120C>T
AA Mutation	p.Arg374Cys(p.R374C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330899
Start	33034222:33034222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650A>G
AA Mutation	p.Lys217Arg(p.K217R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330899
Start	33036613:33036613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773608549
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330899
Start	33026951:33026951(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.276delT
AA Mutation	p.Phe92LeufsTer22(p.F92Lfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000330899
Start	33034329:33034329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751893930
CDS Mutation	c.757C>T
AA Mutation	p.Arg253Ter(p.R253*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330899
Start	33038882:33038883(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1174_1181dupGTTCAGTG
AA Mutation	p.Cys394TrpfsTer25(p.C394Wfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DNAJA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330899
Start	33026825:33026825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145T>G
AA Mutation	p.Ser49Ala(p.S49A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript