Colon Cancer: Gene >> AGPAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336984
Start	32170595:32170595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340A>C
AA Mutation	p.Met114Leu(p.M114L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336984
Start	32169389:32169389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.739G>A
AA Mutation	p.Val247Ile(p.V247I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336984
Start	32169981:32169981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Cys(p.R222C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336984
Start	32169412:32169412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716C>T
AA Mutation	p.Thr239Met(p.T239M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336984
Start	32171063:32171063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.208C>T
AA Mutation	p.Arg70Cys(p.R70C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336984
Start	32169978:32169978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667C>T
AA Mutation	p.Arg223Cys(p.R223C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336984
Start	32170234:32170234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.537A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336984
Start	32169411:32169411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AGPAT1

No Mutation Annotation!