Colon Cancer: Gene >> AIMP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223029
Start	6018013:6018013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.542A>T
AA Mutation	p.Tyr181Phe(p.Y181F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223029
Start	6017836:6017836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764368950
CDS Mutation	c.365T>C
AA Mutation	p.Ile122Thr(p.I122T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000223029
Start	6017932:6017932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75895975
CDS Mutation	c.461C>T
AA Mutation	p.Thr154Met(p.T154M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000223029
Start	6017854:6017854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747974072
CDS Mutation	c.383C>T
AA Mutation	p.Pro128Leu(p.P128L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000223029
Start	6017928:6017928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764843355
CDS Mutation	c.457C>T
AA Mutation	p.His153Tyr(p.H153Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223029
Start	6023580:6023580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223029
Start	6023307:6023307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761471943
CDS Mutation	c.579G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223029
Start	6017870:6017870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.399C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000223029
Start	6017901:6017901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430G>T
AA Mutation	p.Glu144Ter(p.E144*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AIMP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223029
Start	6018006:6018006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750336358
CDS Mutation	c.535C>G
AA Mutation	p.Gln179Glu(p.Q179E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript