Colon Cancer: Gene >> ING2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302327
Start	183510464:183510464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355G>A
AA Mutation	p.Glu119Lys(p.E119K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302327
Start	183510554:183510554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445T>C
AA Mutation	p.Ser149Pro(p.S149P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302327
Start	183510788:183510788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679G>A
AA Mutation	p.Gly227Arg(p.G227R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302327
Start	183505207:183505207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138103277
CDS Mutation	c.12G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302327
Start	183510928:183510928(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.824delA
AA Mutation	p.Lys275ArgfsTer32(p.K275Rfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ING2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302327
Start	183510630:183510630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770426903
CDS Mutation	c.521A>G
AA Mutation	p.Asp174Gly(p.D174G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302327
Start	183510311:183510311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202G>A
AA Mutation	p.Glu68Lys(p.E68K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript