Colon Cancer: Gene >> GRK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392870
Start	119453230:119453230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771181138
CDS Mutation	c.1628C>T
AA Mutation	p.Pro543Leu(p.P543L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392870
Start	119380868:119380868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766100398
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Trp(p.R68W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392870
Start	119436771:119436771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770147450
CDS Mutation	c.859C>T
AA Mutation	p.Arg287Trp(p.R287W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392870
Start	119431468:119431468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.679G>T
AA Mutation	p.Gly227Trp(p.G227W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392870
Start	119453271:119453271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556570876
CDS Mutation	c.1669C>T
AA Mutation	p.Arg557Trp(p.R557W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392870
Start	119436787:119436787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146569660
CDS Mutation	c.875C>T
AA Mutation	p.Ala292Val(p.A292V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392870
Start	119436702:119436702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790A>G
AA Mutation	p.Thr264Ala(p.T264A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392870
Start	119442065:119442065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034G>A
AA Mutation	p.Arg345Gln(p.R345Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392870
Start	119443628:119443628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142G>A
AA Mutation	p.Gly381Asp(p.G381D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392870
Start	119443644:119443644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762466781
CDS Mutation	c.1158C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392870
Start	119425048:119425048(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.501delT
AA Mutation	p.Phe167LeufsTer15(p.F167Lfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GRK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392870
Start	119453157:119453157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555G>A
AA Mutation	p.Glu519Lys(p.E519K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000392870
Start	119454971:119454971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1677T>G
AA Mutation	p.His559Gln(p.H559Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392870
Start	119453228:119453228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1626T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392870
Start	119380843:119380843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.177G>A
Mutation Classification	Silent
Feature Type	Transcript