Colon Cancer: Gene >> ADRA2C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330055
Start	3767102:3767102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Cys(p.R166C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330055
Start	3767012:3767012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406A>G
AA Mutation	p.Thr136Ala(p.T136A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330055
Start	3767123:3767123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517G>A
AA Mutation	p.Val173Met(p.V173M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330055
Start	3767268:3767268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662C>T
AA Mutation	p.Ala221Val(p.A221V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330055
Start	3767741:3767741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1135C>T
AA Mutation	p.Arg379Cys(p.R379C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330055
Start	3767260:3767260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ADRA2C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330055
Start	3767967:3767967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1361G>A
AA Mutation	p.Arg454Gln(p.R454Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript