Colon Cancer: Gene >> KARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302445
Start	75634231:75634231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.857A>G
AA Mutation	p.Tyr286Cys(p.Y286C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302445
Start	75636077:75636077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.504A>T
AA Mutation	p.Glu168Asp(p.E168D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302445
Start	75631852:75631852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919C>T
AA Mutation	p.Leu307Phe(p.L307F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302445
Start	75629513:75629513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1453C>T
AA Mutation	p.Arg485Cys(p.R485C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302445
Start	75631239:75631239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1267C>A
AA Mutation	p.Leu423Ile(p.L423I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302445
Start	75647601:75647601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.39C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KARS

No Mutation Annotation!