Colon Cancer: Gene >> ADRB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305988
Start	148828045:148828045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1214A>T
AA Mutation	p.Asn405Ile(p.N405I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305988
Start	148827858:148827858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027C>T
AA Mutation	p.Arg343Cys(p.R343C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305988
Start	148827180:148827180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>A
AA Mutation	p.Val117Ile(p.V117I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305988
Start	148827155:148827155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.324T>G
AA Mutation	p.Phe108Leu(p.F108L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305988
Start	148827736:148827736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905T>C
AA Mutation	p.Leu302Pro(p.L302P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000305988
Start	148827186:148827186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355G>A
AA Mutation	p.Ala119Thr(p.A119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305988
Start	148827458:148827458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770413972
CDS Mutation	c.627C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305988
Start	148827212:148827212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305988
Start	148827174:148827174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000305988
Start	148827948:148827948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1117G>T
AA Mutation	p.Glu373Ter(p.E373*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ADRB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305988
Start	148827097:148827097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266T>A
AA Mutation	p.Phe89Tyr(p.F89Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305988
Start	148827120:148827120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289A>C
AA Mutation	p.Lys97Gln(p.K97Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript