Colon Cancer: Gene >> GNA11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000078429
Start	3119009:3119009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769503200
CDS Mutation	c.691G>A
AA Mutation	p.Ala231Thr(p.A231T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000078429
Start	3110314:3110314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302A>G
AA Mutation	p.Tyr101Cys(p.Y101C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000078429
Start	3114969:3114969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502G>A
AA Mutation	p.Ala168Thr(p.A168T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000078429
Start	3114957:3114957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775624350
CDS Mutation	c.490G>A
AA Mutation	p.Val164Ile(p.V164I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000078429
Start	3114958:3114958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.491T>C
AA Mutation	p.Val164Ala(p.V164A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000078429
Start	3119328:3119328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000078429
Start	3110300:3110300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000078429
Start	3118936:3118936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.623delG
AA Mutation	p.Gly208AlafsTer16(p.G208Afs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GNA11

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000078429
Start	3118951:3118951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756381542
CDS Mutation	c.633G>A
Mutation Classification	Silent
Feature Type	Transcript