Colon Cancer: Gene >> GNAQ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286548
Start	77815689:77815689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403T>G
AA Mutation	p.Leu135Val(p.L135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286548
Start	77797583:77797583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542G>C
AA Mutation	p.Arg181Thr(p.R181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286548
Start	77797601:77797601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524C>T
AA Mutation	p.Thr175Met(p.T175M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286548
Start	77797577:77797577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397514698
CDS Mutation	c.548G>A
AA Mutation	p.Arg183Gln(p.R183Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286548
Start	77794525:77794525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673T>C
AA Mutation	p.Ser225Pro(p.S225P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000286548
Start	77922330:77922330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.152G>T
AA Mutation	p.Gly51Val(p.G51V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000286548
Start	78031111:78031111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125T>G
AA Mutation	p.Leu42Arg(p.L42R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000286548
Start	77922228:77922228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761634659
CDS Mutation	c.254C>T
AA Mutation	p.Thr85Met(p.T85M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286548
Start	77797549:77797549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286548
Start	77815692:77815695(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.397_400delAAGA
AA Mutation	p.Lys133ValfsTer34(p.K133Vfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000286548
Start	77797578:77797578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547C>T
AA Mutation	p.Arg183Ter(p.R183*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GNAQ

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000286548
Start	77721484:77721484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.919G>T
AA Mutation	p.Glu307Ter(p.E307*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript