Colon Cancer: Gene >> ING3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315870
Start	120968083:120968083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706A>G
AA Mutation	p.Thr236Ala(p.T236A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315870
Start	120967634:120967634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542A>C
AA Mutation	p.Lys181Thr(p.K181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315870
Start	120955566:120955566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769542101
CDS Mutation	c.209A>G
AA Mutation	p.Tyr70Cys(p.Y70C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315870
Start	120967940:120967940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563G>A
AA Mutation	p.Arg188Gln(p.R188Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315870
Start	120968016:120968016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ING3

No Mutation Annotation!