Colon Cancer: Gene >> WARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355338
Start	100369094:100369094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370081524
CDS Mutation	c.92C>T
AA Mutation	p.Ala31Val(p.A31V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355338
Start	100354450:100354450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539C>A
AA Mutation	p.Thr180Lys(p.T180K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355338
Start	100342550:100342550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961A>T
AA Mutation	p.Arg321Trp(p.R321W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355338
Start	100337143:100337143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1173G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WARS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355338
Start	100337189:100337189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760155915
CDS Mutation	c.1127C>T
AA Mutation	p.Ala376Val(p.A376V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355338
Start	100361914:100361914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107T>G
AA Mutation	p.Ile36Ser(p.I36S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript