Colon Cancer: Gene >> ADRA1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306675
Start	159917135:159917135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.230G>A
AA Mutation	p.Arg77Gln(p.R77Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306675
Start	159917065:159917065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160G>A
AA Mutation	p.Ala54Thr(p.A54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306675
Start	159971999:159971999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1070G>A
AA Mutation	p.Arg357His(p.R357H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306675
Start	159917660:159917660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755C>T
AA Mutation	p.Thr252Ile(p.T252I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306675
Start	159917347:159917347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Cys(p.R148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306675
Start	159917433:159917433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.528C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306675
Start	159917490:159917490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306675
Start	159917754:159917754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306675
Start	159917055:159917055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ADRA1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306675
Start	159917134:159917134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571519472
CDS Mutation	c.229C>T
AA Mutation	p.Arg77Trp(p.R77W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306675
Start	159972006:159972006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1077C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306675
Start	159917466:159917466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781618796
CDS Mutation	c.561G>A
Mutation Classification	Silent
Feature Type	Transcript