Colon Cancer: Gene >> GRK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398052
Start	3035435:3035435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747003103
CDS Mutation	c.1319C>T
AA Mutation	p.Ala440Val(p.A440V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398052
Start	3009663:3009663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552G>T
AA Mutation	p.Lys184Asn(p.K184N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398052
Start	3037418:3037418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1452C>A
AA Mutation	p.Phe484Leu(p.F484L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398052
Start	2984536:2984536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146194528
CDS Mutation	c.76C>T
AA Mutation	p.Arg26Cys(p.R26C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398052
Start	2964114:2964114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44C>T
AA Mutation	p.Ala15Val(p.A15V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398052
Start	3019819:3019819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920G>T
AA Mutation	p.Arg307Ile(p.R307I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398052
Start	3022429:3022429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948G>T
AA Mutation	p.Glu316Asp(p.E316D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000398052
Start	3013773:3013773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686A>G
AA Mutation	p.Glu229Gly(p.E229G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398052
Start	3037484:3037484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752841977
CDS Mutation	c.1518G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398052
Start	3035436:3035436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1320G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398052
Start	3019799:3019799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000398052
Start	2992245:2992245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292C>T
AA Mutation	p.Arg98Ter(p.R98*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000398052
Start	3019710:3019711(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.815_816insCCTCTATTT
AA Mutation	p.Asp271_Leu272insPheLeuTyr(p.D271_L272insFLY)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GRK4

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000398052
Start	3035523:3035523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1407T>A
AA Mutation	p.Asp469Glu(p.D469E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398052
Start	3037497:3037497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1531C>A
AA Mutation	p.Pro511Thr(p.P511T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript