Colon Cancer: Gene >> GARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389266
Start	30617154:30617154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1235G>A
AA Mutation	p.Arg412His(p.R412H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389266
Start	30598875:30598875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200887429
CDS Mutation	c.302G>A
AA Mutation	p.Arg101His(p.R101H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389266
Start	30616048:30616048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184C>A
AA Mutation	p.Ala395Asp(p.A395D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389266
Start	30617245:30617245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1326T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389266
Start	30633806:30633806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2166G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389266
Start	30617209:30617209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1290G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389266
Start	30609602:30609602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389266
Start	30633824:30633824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754809551
CDS Mutation	c.2184G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000389266
Start	30628565:30628565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1705G>T
AA Mutation	p.Glu569Ter(p.E569*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GARS

No Mutation Annotation!