Colon Cancer: Gene >> GRK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355472
Start	177440998:177440998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1622G>A
AA Mutation	p.Gly541Asp(p.G541D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355472
Start	177434903:177434903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931G>A
AA Mutation	p.Asp311Asn(p.D311N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355472
Start	177433542:177433542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604G>A
AA Mutation	p.Ala202Thr(p.A202T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355472
Start	177436488:177436488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1362G>T
AA Mutation	p.Lys454Asn(p.K454N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355472
Start	177432021:177432021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.175C>T
AA Mutation	p.Arg59Trp(p.R59W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355472
Start	177436252:177436252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1237T>C
AA Mutation	p.Ser413Pro(p.S413P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355472
Start	177432055:177432055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.209T>G
AA Mutation	p.Phe70Cys(p.F70C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355472
Start	177436138:177436138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123C>A
AA Mutation	p.Leu375Met(p.L375M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355472
Start	177440925:177440925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1549G>A
AA Mutation	p.Glu517Lys(p.E517K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355472
Start	177441753:177441753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1694G>A
AA Mutation	p.Cys565Tyr(p.C565Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GRK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355472
Start	177432754:177432754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.388A>G
AA Mutation	p.Thr130Ala(p.T130A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript