Colon Cancer: Gene >> GNA12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275364
Start	2731522:2731522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805C>T
AA Mutation	p.Arg269Trp(p.R269W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275364
Start	2731534:2731534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793A>G
AA Mutation	p.Arg265Gly(p.R265G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275364
Start	2731302:2731302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140322696
CDS Mutation	c.1025G>A
AA Mutation	p.Arg342His(p.R342H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000275364
Start	2731530:2731530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758369709
CDS Mutation	c.797G>A
AA Mutation	p.Arg266His(p.R266H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275364
Start	2731496:2731496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275364
Start	2731511:2731511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275364
Start	2731664:2731664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275364
Start	2731271:2731271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138692914
CDS Mutation	c.1056C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000275364
Start	2795119:2795119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334C>T
AA Mutation	p.Arg112Ter(p.R112*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000275364
Start	2733469:2733470(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.557dupT
AA Mutation	p.Leu186PhefsTer12(p.L186Ffs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GNA12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275364
Start	2794978:2794978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475A>G
AA Mutation	p.Arg159Gly(p.R159G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript