Colon Cancer: Gene >> RGS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367909
Start	163073492:163073492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248A>G
AA Mutation	p.Glu83Gly(p.E83G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367909
Start	163073575:163073575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567536966
CDS Mutation	c.331G>A
AA Mutation	p.Ala111Thr(p.A111T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367909
Start	163072414:163072414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771715416
CDS Mutation	c.64C>T
AA Mutation	p.Arg22Trp(p.R22W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367909
Start	163074427:163074427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.485A>G
AA Mutation	p.Lys162Arg(p.K162R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367909
Start	163073602:163073602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.358T>G
AA Mutation	p.Ser120Ala(p.S120A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367909
Start	163073478:163073478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367909
Start	163073578:163073578(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.338delA
AA Mutation	p.Lys113ArgfsTer15(p.K113Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RGS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367909
Start	163072408:163072408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58A>G
AA Mutation	p.Lys20Glu(p.K20E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367909
Start	163074518:163074518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript