Colon Cancer: Gene >> GNAI2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000313601
Start	50257500:50257500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.878G>A
AA Mutation	p.Gly293Glu(p.G293E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313601
Start	50252435:50252435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781986131
CDS Mutation	c.200G>A
AA Mutation	p.Arg67Gln(p.R67Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313601
Start	50257677:50257677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055G>A
AA Mutation	p.Cys352Tyr(p.C352Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313601
Start	50257604:50257604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.982A>T
AA Mutation	p.Thr328Ser(p.T328S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313601
Start	50252524:50252524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782148570
CDS Mutation	c.289G>A
AA Mutation	p.Asp97Asn(p.D97N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313601
Start	50257588:50257588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377114196
CDS Mutation	c.966G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313601
Start	50252439:50252439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313601
Start	50256270:50256270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GNAI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313601
Start	50256759:50256759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630G>T
AA Mutation	p.Lys210Asn(p.K210N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313601
Start	50256966:50256966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781818717
CDS Mutation	c.753C>T
Mutation Classification	Silent
Feature Type	Transcript