Colon Cancer: Gene >> ING4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396807
Start	6652699:6652699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.463C>A
AA Mutation	p.Pro155Thr(p.P155T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396807
Start	6652764:6652764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374663258
CDS Mutation	c.398G>A
AA Mutation	p.Arg133Gln(p.R133Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396807
Start	6652692:6652692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470C>T
AA Mutation	p.Thr157Ile(p.T157I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396807
Start	6652712:6652712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201626425
CDS Mutation	c.450G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000396807
Start	6652312:6652312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607C>T
AA Mutation	p.Gln203Ter(p.Q203*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ING4

No Mutation Annotation!