Colon Cancer: Gene >> RGS18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367460
Start	192184444:192184444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598G>T
AA Mutation	p.Asp200Tyr(p.D200Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367460
Start	192184469:192184469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623G>T
AA Mutation	p.Arg208Ile(p.R208I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367460
Start	192158751:192158751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114A>C
AA Mutation	p.Lys38Asn(p.K38N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367460
Start	192184437:192184437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000367460
Start	192184321:192184321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.475G>T
AA Mutation	p.Glu159Ter(p.E159*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000367460
Start	192158743:192158743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106G>T
AA Mutation	p.Glu36Ter(p.E36*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367460
Start	192158709:192158710(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.76_77insTATTCCATACATATAC
AA Mutation	p.His26LeufsTer22(p.H26Lfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RGS18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367460
Start	192184364:192184364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518T>G
AA Mutation	p.Phe173Cys(p.F173C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript