Colon Cancer: Gene >> IGF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300632
Start	2133633:2133633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762200142
CDS Mutation	c.190C>T
AA Mutation	p.Arg64Cys(p.R64C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300632
Start	2135444:2135444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80G>A
AA Mutation	p.Arg27His(p.R27H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000300632
Start	2133518:2133518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369122420
CDS Mutation	c.305C>T
AA Mutation	p.Pro102Leu(p.P102L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300632
Start	2135381:2135381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143G>A
AA Mutation	p.Arg48His(p.R48H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300632
Start	2133661:2133661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.162G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300632
Start	2133529:2133529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300632
Start	2133012:2133012(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.518delC
AA Mutation	p.Pro173GlnfsTer27(p.P173Qfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300632
Start	2133021:2133021(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.509delG
AA Mutation	p.Gly170AlafsTer30(p.G170Afs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300632
Start	2133011:2133012(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs755455183
CDS Mutation	c.518dupC
AA Mutation	p.Glu174ArgfsTer50(p.E174Rfs*50)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IGF2

No Mutation Annotation!